(1S,6S)-6-{[2-(1H-Indol-3-yl)-ethylcarbamoyl]-methyl}-cyclohex-3-enecarboxylic acid methyl ester

Base Information

Chemical Name:(1S,6S)-6-{[2-(1H-Indol-3-yl)-ethylcarbamoyl]-methyl}-cyclohex-3-enecarboxylic acid methyl ester
CAS No.:74207-05-9
Molecular Formula:C₂₀H₂₄N₂O₃
Molecular Weight:340.422
Hs Code.:

Synonyms:(1S,6S)-6-{[2-(1H-Indol-3-yl)-ethylcarbamoyl]-methyl}-cyclohex-3-enecarboxylic acid methyl ester

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Chemical Property of (1S,6S)-6-{[2-(1H-Indol-3-yl)-ethylcarbamoyl]-methyl}-cyclohex-3-enecarboxylic acid methyl ester

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Technology Process of (1S,6S)-6-{[2-(1H-Indol-3-yl)-ethylcarbamoyl]-methyl}-cyclohex-3-enecarboxylic acid methyl ester

There total 2 articles about (1S,6S)-6-{[2-(1H-Indol-3-yl)-ethylcarbamoyl]-methyl}-cyclohex-3-enecarboxylic acid methyl ester which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 80.6%

: 61-54-1
tryptamine

: 74207-04-8
methyl cis-6-<(diazomethyl)carbonyl>-3-cyclohexene-1-carboxylate

: 74207-05-9
(1S,6S)-6-{[2-(1H-Indol-3-yl)-ethylcarbamoyl]-methyl}-cyclohex-3-enecarboxylic acid methyl ester

Guidance literature:: With silver(l) oxide; In 1,4-dioxane; for 0.333333h; Ambient temperature;
DOI:10.1016/S0040-4020(01)98879-9

Reference yield:

: 74207-05-9
(1S,6S)-6-{[2-(1H-Indol-3-yl)-ethylcarbamoyl]-methyl}-cyclohex-3-enecarboxylic acid methyl ester

Guidance literature:: /BRN= 403680/ (2), Tryptamin, Ag2O;

Reference yield:

: 74207-05-9
(1S,6S)-6-{[2-(1H-Indol-3-yl)-ethylcarbamoyl]-methyl}-cyclohex-3-enecarboxylic acid methyl ester

: 74207-07-1,74243-36-0,111561-00-3
dihydrooxoyohimbane

: 74243-35-9
1-(1,2,3,6-tetrahydro-2-methoxycarbonylbenzyl)-1,2,3,4-tetrahydro-β-carboline hydrochloride

Guidance literature:: With sodium tetrahydroborate; trichlorophosphate; Yield given. Multistep reaction. Yields of byproduct given; 1.) benzene, 3 h., reflux; 2.) methanol, 10 min., room temp.;
DOI:10.1016/S0040-4020(01)98879-9