methyl β-<(benzoyloxy)methyl>-β,7-diethyl-3-(methylthio)-1H-indole-2-propanoate

Base Information

Chemical Name:methyl β-<(benzoyloxy)methyl>-β,7-diethyl-3-(methylthio)-1H-indole-2-propanoate
CAS No.:122761-97-1
Molecular Formula:C₂₅H₂₉NO₄S
Molecular Weight:439.576
Hs Code.:

Synonyms:methyl β-<(benzoyloxy)methyl>-β,7-diethyl-3-(methylthio)-1H-indole-2-propanoate

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of methyl β-<(benzoyloxy)methyl>-β,7-diethyl-3-(methylthio)-1H-indole-2-propanoate

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Technology Process of methyl β-<(benzoyloxy)methyl>-β,7-diethyl-3-(methylthio)-1H-indole-2-propanoate

There total 4 articles about methyl β-<(benzoyloxy)methyl>-β,7-diethyl-3-(methylthio)-1H-indole-2-propanoate 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:

: Benzoic acid 2-carboxymethyl-2-ethyl-3-oxo-butyl ester

: 122761-97-1
methyl β-<(benzoyloxy)methyl>-β,7-diethyl-3-(methylthio)-1H-indole-2-propanoate

Guidance literature:: Multi-step reaction with 4 steps

1: diethyl ether

2: 96 percent / bromine / methanol / 1 h / Ambient temperature

3: 64 percent / toluene / 1) 1 d, 67 deg C, 2) 1 d, 70 deg C, 3) 1 d, 77 deg C

4: 1) t-BuOCl, 2) triethylamine / 1) CH₃CN, CH₂Cl₂, 1 h, 2) 30 min, r,t,

With tert-butylhypochlorite; bromine; triethylamine; In methanol; diethyl ether; toluene;
DOI:10.1021/jm00129a018

Reference yield:

: 122761-95-9
methyl 3-<(benzoyloxy)methyl>-5-bromo-3-ethyl-4-oxopentanoate

: 122761-97-1
methyl β-<(benzoyloxy)methyl>-β,7-diethyl-3-(methylthio)-1H-indole-2-propanoate

Guidance literature:: Multi-step reaction with 2 steps

1: 64 percent / toluene / 1) 1 d, 67 deg C, 2) 1 d, 70 deg C, 3) 1 d, 77 deg C

2: 1) t-BuOCl, 2) triethylamine / 1) CH₃CN, CH₂Cl₂, 1 h, 2) 30 min, r,t,

With tert-butylhypochlorite; triethylamine; In toluene;
DOI:10.1021/jm00129a018

Reference yield:

: 122761-92-6
methyl 3-<(benzoyloxy)methyl>-3-ethyl-4-oxopentanoate

: 122761-97-1
methyl β-<(benzoyloxy)methyl>-β,7-diethyl-3-(methylthio)-1H-indole-2-propanoate

Guidance literature:: Multi-step reaction with 3 steps

1: 96 percent / bromine / methanol / 1 h / Ambient temperature

2: 64 percent / toluene / 1) 1 d, 67 deg C, 2) 1 d, 70 deg C, 3) 1 d, 77 deg C

3: 1) t-BuOCl, 2) triethylamine / 1) CH₃CN, CH₂Cl₂, 1 h, 2) 30 min, r,t,

With tert-butylhypochlorite; bromine; triethylamine; In methanol; toluene;
DOI:10.1021/jm00129a018