(Z)-7-[(1S,2R,3R,4R)-3-({2-[2-(4-tert-Butyl-phenylsulfanyl)-acetylamino]-acetylamino}-methyl)-7-oxa-bicyclo[2.2.1]hept-2-yl]-hept-5-enoic acid

Base Information

Chemical Name:(Z)-7-[(1S,2R,3R,4R)-3-({2-[2-(4-tert-Butyl-phenylsulfanyl)-acetylamino]-acetylamino}-methyl)-7-oxa-bicyclo[2.2.1]hept-2-yl]-hept-5-enoic acid
CAS No.:128781-25-9
Molecular Formula:C₂₈H₄₀N₂O₅S
Molecular Weight:516.702
Hs Code.:

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Chemical Property of (Z)-7-[(1S,2R,3R,4R)-3-({2-[2-(4-tert-Butyl-phenylsulfanyl)-acetylamino]-acetylamino}-methyl)-7-oxa-bicyclo[2.2.1]hept-2-yl]-hept-5-enoic acid

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Technology Process of (Z)-7-[(1S,2R,3R,4R)-3-({2-[2-(4-tert-Butyl-phenylsulfanyl)-acetylamino]-acetylamino}-methyl)-7-oxa-bicyclo[2.2.1]hept-2-yl]-hept-5-enoic acid

There total 5 articles about (Z)-7-[(1S,2R,3R,4R)-3-({2-[2-(4-tert-Butyl-phenylsulfanyl)-acetylamino]-acetylamino}-methyl)-7-oxa-bicyclo[2.2.1]hept-2-yl]-hept-5-enoic acid 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:

: (Z)-7-[(1S,2R,3R,4R)-3-({2-[2-(4-tert-Butyl-phenylsulfanyl)-acetylamino]-acetylamino}-methyl)-7-oxa-bicyclo[2.2.1]hept-2-yl]-hept-5-enoic acid methyl ester

: 128781-25-9
(Z)-7-[(1S,2R,3R,4R)-3-({2-[2-(4-tert-Butyl-phenylsulfanyl)-acetylamino]-acetylamino}-methyl)-7-oxa-bicyclo[2.2.1]hept-2-yl]-hept-5-enoic acid

Guidance literature:: With lithium hydroxide; In tetrahydrofuran; for 2.5h; Yield given; Ambient temperature;
DOI:10.1021/jm00171a021

Reference yield:

: 128781-39-5
N-<<(4-tert-butylphenyl)thio>acetyl>glycine

: 128781-25-9
(Z)-7-[(1S,2R,3R,4R)-3-({2-[2-(4-tert-Butyl-phenylsulfanyl)-acetylamino]-acetylamino}-methyl)-7-oxa-bicyclo[2.2.1]hept-2-yl]-hept-5-enoic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) N,N'-carbonyldiimidazole / 1.) a) THF, 0 deg C, 1 h, b) RT, 1 h, 2.) RT, overnight

2: 1 N aq. LiOH / tetrahydrofuran / 2.5 h / Ambient temperature

With lithium hydroxide; 1,1'-carbonyldiimidazole; In tetrahydrofuran;
DOI:10.1021/jm00171a021

Reference yield:

: 107437-27-4
(Z)-7-[(1S,2R,3R,4R)-3-(1,3-Dioxo-1,3-dihydro-isoindol-2-ylmethyl)-7-oxa-bicyclo[2.2.1]hept-2-yl]-hept-5-enoic acid methyl ester

: 128781-25-9
(Z)-7-[(1S,2R,3R,4R)-3-({2-[2-(4-tert-Butyl-phenylsulfanyl)-acetylamino]-acetylamino}-methyl)-7-oxa-bicyclo[2.2.1]hept-2-yl]-hept-5-enoic acid

Guidance literature:: Multi-step reaction with 3 steps

1: 71 percent / hydrazine / CH₂Cl₂; ethanol / 23 h / Ambient temperature

2: 1.) N,N'-carbonyldiimidazole / 1.) a) THF, 0 deg C, 1 h, b) RT, 1 h, 2.) RT, overnight

3: 1 N aq. LiOH / tetrahydrofuran / 2.5 h / Ambient temperature

With lithium hydroxide; 1,1'-carbonyldiimidazole; hydrazine; In tetrahydrofuran; ethanol; dichloromethane;
DOI:10.1021/jm00171a021