3-(1-benzyloxycarbonylamino-ethyl)-5-methyl-isoxazole-4-carboxylic acid tert-butyl ester

Base Information

Chemical Name:3-(1-benzyloxycarbonylamino-ethyl)-5-methyl-isoxazole-4-carboxylic acid tert-butyl ester
CAS No.:237765-43-4
Molecular Formula:C₁₉H₂₄N₂O₅
Molecular Weight:360.41
Hs Code.:

3-(1-benzyloxycarbonylamino-ethyl)-5-methyl-isoxazole-4-carboxylic acid <i>tert</i>-butyl ester

Synonyms:3-(1-benzyloxycarbonylamino-ethyl)-5-methyl-isoxazole-4-carboxylic acid tert-butyl ester

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Chemical Property of 3-(1-benzyloxycarbonylamino-ethyl)-5-methyl-isoxazole-4-carboxylic acid tert-butyl ester

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Technology Process of 3-(1-benzyloxycarbonylamino-ethyl)-5-methyl-isoxazole-4-carboxylic acid tert-butyl ester

There total 1 articles about 3-(1-benzyloxycarbonylamino-ethyl)-5-methyl-isoxazole-4-carboxylic acid tert-butyl 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:

: tert-butyl 3-(pyrrolidin-1-yl)but-2-enoate

: C₁₁H₁₃ClN₂O₃

: 237765-43-4
3-(1-benzyloxycarbonylamino-ethyl)-5-methyl-isoxazole-4-carboxylic acid tert-butyl ester

Guidance literature:: With triethylamine; In chloroform; Yield given; Heating;
DOI:10.1055/s-1999-3091

Reference yield: 96.0%

: 237765-43-4
3-(1-benzyloxycarbonylamino-ethyl)-5-methyl-isoxazole-4-carboxylic acid tert-butyl ester

: 237765-50-3
3-((S)-1-Benzyloxycarbonylamino-ethyl)-5-methyl-isoxazole-4-carboxylic acid

Guidance literature:: With trifluoroacetic acid; In dichloromethane; at 0 ℃; for 3h;
DOI:10.1055/s-1999-3091

Reference yield:

: 237765-43-4
3-(1-benzyloxycarbonylamino-ethyl)-5-methyl-isoxazole-4-carboxylic acid tert-butyl ester

: 237765-54-7
C₁₈H₂₀N₂O₇

Guidance literature:: Multi-step reaction with 2 steps

1: 96 percent / TFA / CH₂Cl₂ / 3 h / 0 °C

2: Et₃N / tetrahydrofuran / 16 h / 0 - 20 °C

With triethylamine; trifluoroacetic acid; In tetrahydrofuran; dichloromethane;
DOI:10.1055/s-1999-3091