[(S)-1-((1R,2S)-2-Diethylcarbamoyl-2-phenyl-cyclopropyl)-allyl]-carbamic acid tert-butyl ester

Base Information

Chemical Name:[(S)-1-((1R,2S)-2-Diethylcarbamoyl-2-phenyl-cyclopropyl)-allyl]-carbamic acid tert-butyl ester
CAS No.:171889-33-1
Molecular Formula:C₂₂H₃₂N₂O₃
Molecular Weight:372.508
Hs Code.:

Synonyms:[(S)-1-((1R,2S)-2-Diethylcarbamoyl-2-phenyl-cyclopropyl)-allyl]-carbamic acid tert-butyl ester

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Chemical Property of [(S)-1-((1R,2S)-2-Diethylcarbamoyl-2-phenyl-cyclopropyl)-allyl]-carbamic acid tert-butyl ester

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Technology Process of [(S)-1-((1R,2S)-2-Diethylcarbamoyl-2-phenyl-cyclopropyl)-allyl]-carbamic acid tert-butyl ester

There total 15 articles about [(S)-1-((1R,2S)-2-Diethylcarbamoyl-2-phenyl-cyclopropyl)-allyl]-carbamic 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: 95.0%

: 171889-32-0
[(S)-1-((1R,2S)-2-Diethylcarbamoyl-2-phenyl-cyclopropyl)-3-phenylselanyl-propyl]-carbamic acid tert-butyl ester

: 171889-33-1
[(S)-1-((1R,2S)-2-Diethylcarbamoyl-2-phenyl-cyclopropyl)-allyl]-carbamic acid tert-butyl ester

Guidance literature:: With dihydrogen peroxide; In tetrahydrofuran; for 120h; Ambient temperature;
DOI:10.1021/jm960495w

Reference yield:

: 24424-99-5
di-tert-butyl dicarbonate

: 171889-33-1
[(S)-1-((1R,2S)-2-Diethylcarbamoyl-2-phenyl-cyclopropyl)-allyl]-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 96 percent / acetonitrile / 1.5 h / Ambient temperature

2: 60 percent / DIBAL-H / tetrahydrofuran / 1.) -78 deg C, 1 h, 2.) RT, 15 h

3: 1.) oxalyl chloride, DMSO, 2.) Et₃N / 1.) CH₂Cl₂, -78 deg C, 2 h, 2.) CH₂Cl₂, -78 deg C, 1 h

4: 1.) BuLi / 1.) THF, hexane, -21 deg C, 30 min, 2.) THF, -21 deg C, 1.5 h

With n-butyllithium; oxalyl dichloride; diisobutylaluminium hydride; dimethyl sulfoxide; triethylamine; In tetrahydrofuran; acetonitrile;
DOI:10.1021/jm980238m

Reference yield:

: 213018-89-4
(R)-tert-Butoxycarbonylamino-((1R,2S)-2-diethylcarbamoyl-2-phenyl-cyclopropyl)-acetic acid methyl ester

: 171889-33-1
[(S)-1-((1R,2S)-2-Diethylcarbamoyl-2-phenyl-cyclopropyl)-allyl]-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 60 percent / DIBAL-H / tetrahydrofuran / 1.) -78 deg C, 1 h, 2.) RT, 15 h

2: 1.) oxalyl chloride, DMSO, 2.) Et₃N / 1.) CH₂Cl₂, -78 deg C, 2 h, 2.) CH₂Cl₂, -78 deg C, 1 h

3: 1.) BuLi / 1.) THF, hexane, -21 deg C, 30 min, 2.) THF, -21 deg C, 1.5 h

With n-butyllithium; oxalyl dichloride; diisobutylaluminium hydride; dimethyl sulfoxide; triethylamine; In tetrahydrofuran;
DOI:10.1021/jm980238m