- •#3 Aleph; dot; para-dot; 2,5-dimethoxy-4-methylthioamphetamine
- •#4 Aleph-2; 2,5-dimethoxy-4-ethylthioamphetamine
- •#5 Aleph-4; 2,5-dimethoxy-4-(I)-propylthioamphetamine
- •#6 Aleph-6 2,5-dimethoxy-4-phenylthioamphetamine
- •#7 Aleph-7; 2,5-dimethoxy-4-(n)-propylthioamphetamine
- •#8 Ariadne; 4c-dom; bl-3912; dimoxamine; 1-(2,5-dimethoxy-4-methylphenyl)-2-aminobutane; 2,5-dimethoxy-a-ethyl-4-methylphenethylamine
- •#9 Asb; asymbescaline; 3,4-diethoxy-5-methoxyphenethylamine
- •#10 B; buscaline; 4-(n)-butoxy-3,5-dimethoxyphenethylamine
- •#11 Beatrice; n-methyl-dom; 2,5-dimethoxy-4,n-dimethylamphetamine
- •#13 Bob; beta-methoxy-2c-b; 4-bromo-2,5-beta-trimethoxyphenethylamine
- •#14 Bod; beta-methoxy-2c-d; 4-methyl-2,5,beta-trimethoxyphenethylamine
- •#15 Boh; beta-methoxy-3,4-methylenedioxyphenethylamine
- •#16 Bohd; 2,5-dimethoxy-beta-hydroxy-4-methylphenethylamine
- •#17 Bom; beta-methoxymescaline; 3,4,5,beta-tetramethoxyphenethylamine
- •#37 Cpm; cyclopropylmescaline;
- •#42 Gamma-2c-t-4; 2,6-dimethoxy-4-(I)-propylthiophenethylamine)
- •#51 Beta-d; 3,4,5-trimethoxy-beta,beta-dideuterophenethylamine
- •#52 Desoxy; 3,5-dimethoxy-4-methylphenethylamine
- •#56 Dmcpa; 2-(2,5-dimethoxy-4-methylphenyl)cyclopropylamine
- •#58 Dmmda; 2,5-dimethoxy-3,4-methylenedioxyamphetamine
- •#59 Dmmda-2; 2,3-dimethoxy-4,5-methylenedioxyamphetamine
- •#60 Dmpea; 3,4-dimethoxyphenethylamine
- •#61 Doam; 2,5-dimethoxy-4-(n)-amylamphetamine
- •#63 Dobu; 2,5-dimethoxy-4-(n)-butylamphetamine
- •#65 Doef; 2,5-dimethoxy-4-(2-fluoroethyl)-
- •#66 Doet; hecate; 2,5-dimethoxy-4-ethylamphetamine
- •#68 Dom; stp; 2,5-dimethoxy-4-methylamphetamine
- •#69 Gamma-dom; z-7; 2,6-dimethoxy-4-methylamphetamine
- •#71 Dopr; 2,5-dimethoxy-4-(n)-propylamphetamine
- •#72 E; escaline; 3,5-dimethoxy-4-ethoxyphenethylamine
- •#73 Eee; 2,4,5-triethoxyamphetamine
- •#77 Ethyl-j; 2-ethylamino-1-(3,4-methylenedioxyphenyl)butane; n-ethyl-1-(1,3-benzodioxol-5-yl)-2-butanamine
- •#81 Flea; n-hydroxy-n-methyl-3,4-methylenedioxyamphetamine
- •#85 Ganesha; g; 2,5-dimethoxy-3,4-dimethylamphetamine
- •#90 Idnna; 2,5-dimethoxy-n,n-dimethyl-4-iodoamphetamine
- •#91 Im; isomescaline; 2,3,4-trimethoxyphenethylamine
- •#92 Ip; isoproscaline; 3,5-dimethoxy-4-(I)-propoxyphenethylamine
- •#93 Iris; 5-ethoxy-2-methoxy-4-methylamphetamine
- •#94 J; bdb; 2-amino-1-(3,4-methylenedioxyphenyl)butane;
- •#95 Lophophine; 3-methoxy-4,5-methylenedioxyphenethylamine
- •#96 M; mescaline; 3,4,5-trimethoxyphenethylamine
- •#98 Madam-6; 2,n-dimethyl-4,5-methylenedioxyamphetamine
- •#99 Mal; methallylescaline;
- •#100 Mda; 3,4-methylenedioxyamphetamine
- •#101 Mdal; n-allyl-mda; 3,4-methylenedioxy-n- allylamphetamine
- •#102 Mdbu; n-butyl-mda; 3,4-methylenedioxy-n-butylamphetamine
- •#103 Mdbz; n-benzyl-mda; 3,4-methylenedioxy-n-benzylamphetamine
- •#104 Mdcpm; cyclopropylmethyl-mda;
- •#105 Mddm; n,n-dimethyl-mda;
- •#106 Mde; mdea; eve; n-ethyl-mda;
- •#107 Mdhoet; hydroxyethyl-mda;
- •#109 Mdma; mdm; adam; ecstasy; 3,4-methylenedioxy-n-methylamphetamine
- •#110 Mdmc; edma; 3,4-ethylenedioxy-n-methylamphetamine
- •#111 Mdmeo; n-methoxy-mda; 3,4-methylenedioxy-n-methyoxyamphetamine
- •#112 Mdmeoet; n-methoxyethyl-mda;
- •#114 Mdoh; n-hydroxy-mda; 3,4-methylenedioxy-n-hydroxyamphetamine
- •I would put my money on the likelihood of mda going to mdoh if it
- •#115 Mdpea; 3,4-methylenedioxyphenethylamine; homopiperonylamine
- •#116 Mdph; a,a-dimethyl-3,4-methylenedioxy-
- •In symbolic form this is:
- •#117 Mdpl; n-propargyl-mda; n-propynyl-mda;
- •#118 Mdpr; n-propyl-mda; 3,4-methylenedioxy-n-propylamphetamine
- •#119 Me; metaescaline; 3,4-dimethoxy-5-ethoxyphenethylamine
- •#120 Meda; 3-methoxy-4,5-ethylenedioxyamphetamine
- •#121 Mee; 4,5-diethoxy-2-methoxyamphetamine
- •#122 Mem; 2,5-dimethoxy-4-ethoxyamphetamine
- •#123 Mepea; 3-methoxy-4-ethoxyphenethylamine
- •#124 Meta-dob; 5-bromo-2,4-dimethoxyamphetamine
- •#125 Meta-dot; 2,4-dimethoxy-5-methylthioamphetamine
- •#126 Methyl-dma; dmma; 2,5-dimethoxy-n-methylamphetamine
- •#127 Methyl-dob; 4-bromo-2,5-dimethoxy-n-methylamphetamine
- •#130 Methyl-ma; pmma; doone; 4-mma; 4-methoxy-n-methylamphetamine
- •#131 Methyl-mmda-2; 2-methoxy-n-methyl-4,5-methylenedioxyamphetamine
- •#132 Mmda; 3-methoxy-4,5-methylenedioxyamphetamine
- •#133 Mmda-2; 2-methoxy-4,5-methylenedioxyamphetamine
- •#134 Mmda-3a; 2-methoxy-3,4-methylenedioxyamphetamine
- •#135 Mmda-3b; 4-methoxy-2,3-methylenedioxyamphetamine
- •#136 Mme; 2,4-dimethoxy-5-ethoxyamphetamine
- •#137 Mp; metaproscaline; 3,4-dimethoxy-5-(n)-propoxyphenethylamine
- •#138 Mpm; 2,5-dimethoxy-4-(n)-propoxyamphetamine
- •#139 Ortho-dot; 4,5-dimethoxy-2-methylthioamphetamine
- •#140 P; proscaline; 3,5-dimethoxy-4-(n)-propoxyphenethylamine
- •#141 Pe; phenescaline; 3,5-dimethoxy-4-phenethyloxyphenethylamine
- •#142 Pea; phenethylamine
- •#143 Propynyl; 3,5-dimethoxy-4-(2-propynyloxy)phenethylamine
- •#144 Sb; symbescaline; 3,5-diethoxy-4-methoxyphenethylamine
- •#145 Ta; 2,3,4,5-tetramethoxyamphetamine
- •#146 3-Tasb; 3-thioasymbescaline;
- •#147 4-Tasb; 4-thioasymbescaline;
- •#148 5-Tasb; 5-thioasymbescaline;
- •#149 Tb; 4-thiobuscaline; 3,5-dimethoxy-4-(n)-butylthiophenethylamine
- •#150 3-Te; 3-thioescaline;
- •#151 Te; 4-te; 4-thioescaline; 3,5-dimethoxy-4-ethylthiophenethylamine
- •#153 3-Tim; 3-thiomescaline; 2,4-dimethoxy-3-methylthiophenethylamine
- •#154 4-Tim; 4-thioisomescaline;
- •#155 3-Tm; 3-thiomescaline; 3,4-dimethoxy-5-methylthiophenethylamine
- •#156 Tm; 4-tm; 4-thiomescaline;
- •#157 Tma; 3,4,5-trimethoxyamphetamine
- •#158 Tma-2; 2,4,5-trimethoxyamphetamine
- •#159 Tma-3; 2,3,4-trimethoxyamphetamine
- •#160 Tma-4; 2,3,5-trimethoxyamphetamine
- •#161 Tma-5; 2,3,6-trimethoxyamphetamine
- •#162 Tma-6; 2,4,6-trimethoxyamphetamine
- •#163 3-Tme; 3-thiometaescaline;
- •#164 4-Tme; 4-thiometaescaline;
- •#165 5-Tme; 5-thiometaescaline;
- •#166 2T-mmda-3a; 3,4-methylenedioxy-2-methylthioamphetamine
- •#167 4T-mmda-2; 6-(2-aminopropyl)-5-methoxy-1,3-benzoxathiol;
- •#168 Tmpea; 2,4,5-trimethoxyphenethylamine
- •#169 2-Toet; 4-ethyl-5-methoxy-2-methylthioamphetamine
- •#170 5-Toet; 4-ethyl-2-methoxy-5-methylthioamphetamine
- •#171 2-Tom; 5-methoxy-4-methyl-2-methylthioamphetamine
- •#172 5-Tom; 2-methoxy-4-methyl-5-methylthioamphetamine
- •#173 Tomso; 2-methoxy-4-methyl-5-methylsulfinylamphetamine
- •#174 Tp; thioproscaline; 3,5-dimethoxy-4-(n)-propylthiophenethylamine
- •#175 Tris; trescaline; trisescaline; 3,4,5-triethoxyphenethylamine
- •#176 3-Tsb; 3-thiosymbescaline;
- •#177 4-Tsb; 4-thiosymbescaline;
- •#178 3-T-tris; 3-thiotrescaline; 3-thiotrisescaline;
- •#179 4-T-tris; 4-thiotrescaline; 4-thiotrisescaline;
#153 3-Tim; 3-thiomescaline; 2,4-dimethoxy-3-methylthiophenethylamine
SYNTHESIS: A mixture of 3.1 g POCl3 2.8 g N-methylformanilide was heated on a steam bath until it was a deep claret color (about 5 min). To this there was then added 3.0 g of 2,6-dimethoxythioanisole (see under 4-TM for its preparation), and heating was continued for 30 min. The reaction mixture was then added to 75 mL H2O and stirred overnight. The dark oily mixture was extracted with 3x75 mL CH2Cl2, the extracts pooled, and the solvent removed under vacuum. The residue was extracted with 3x20 mL boiling hexane, each extract being poured off from the insoluble residue. Pooling and cooling these extracts yielded 1.5 g of 2,4-dimethoxy-3-(methylthio)benzaldehyde as an off-white crystalline solid with a mp of 67-69 deg C. Recrystallization from either MeOH or cyclohexane tightened the mp, but lowered it to 67-68 deg C and 66-67 deg C, resp. Anal. (C10H12O3S) C,H.
To a solution of 1.3 g 2,4-dimethoxy-3-(methylthio)benzaldehyde in 60 mL nitromethane there was added 0.3 g anhydrous ammonium acetate and the mixture was heated at reflux for 3 h. The hot solution was decanted from a little insoluble material, and the excess nitromethane was removed under vacuum. The residue dissolved in 10 mL hot MeOH. On cooling, yellow crystals of 2,4-dimethoxy-3-methylthio-beta-nitrostyrene were obtained which were removed by filtration and air-dried, and weighed 0.9 g. The mp was 130-133 deg C and could be improved to 136-137 deg C following recrystallization from MeOH (10 g/g). Anal. (C11H13NO4S) C,H.
A well-stirred solution of 0.6 g LAH in 10 mL anhydrous THF was cooled to 0 deg C under He. There was added, dropwise, 0.4 mL of 100% H2SO4, followed by 0.6 g of 2,4-dimethoxy-3-methylthio-beta-nitrostyrene dissolved in a little THF. Stirring was continued for a few min as the reaction returned to room temperature, and then it was heated to a reflux for 5 min on the steam bath. The reaction was cooled again, and 25% NaOH was added dropwise until a white granular precipitate was obtained. This was removed by filtration, and the filter cake was washed with 2x25 mL Et2O. The filtrate was extracted into 25 mL dilute H2SO4 which was, in turn, made basic again and extracted with 2x25 mL CH2Cl2. The extracts were pooled, and the solvent removed under vacuum to give a residue of crude product. This was distilled from 120-140 deg C at 0.3 mm/Hg yielding 0.25 g of a clear white oil. This was dissolved in 5 mL IPA, neutralized with about 3 drops of concentrated HCl, and diluted with 15 mL anhydrous Et2O. Scratching with a glass rod instigated crystallization of bright white solids which were filtered, washed with Et2O, and air dried. The weight of 2,4-dimethoxy-3-methylthiophenethylamine hydrochloride (3-TIM) was 0.2 g and the mp was 204-206 deg C with decomposition. This hydrochloride appeared to be a hemihydrate. Anal. (C11H18ClNO2Sa1/2 H2O) C,H,N.
DOSAGE: greater than 240 mg.
DURATION: unknown.
QUALITATIVE COMMENTS: (with 240 mg) Briefly I thought that there might have been an alert at the 2 to 3 hour point, but I now think it was nothing. During the following day I had a mild stomach upset off and on, but I can't believe that it was connected with 3-TIM.
EXTENSIONS AND COMMENTARY: Isomescaline itself is not active, but there is no way of knowing just how "non-active" it really is. If it were to be active just beyond the levels assayed, then the introduction of a sulfur into the molecule in place of an oxygen could have increased the potency to where it might have some effect. The absence of any activity from this TIM, and the other two TIMs, might well suggest that isomescaline is really very "non-active," if that makes sense!