[((S)-1-Cyano-2-phenyl-ethylcarbamoyl)-methyl]-carbamic acid tert-butyl ester

Base Information

• Chemical Name: [((S)-1-Cyano-2-phenyl-ethylcarbamoyl)-methyl]-carbamic acid tert-butyl ester
• CAS No.: 99281-91-1
• Molecular Formula: C₁₆H₂₁N₃O₃
• Molecular Weight: 303.361

Synonyms:[((S)-1-Cyano-2-phenyl-ethylcarbamoyl)-methyl]-carbamic acid tert-butyl ester

Chemical Property of [((S)-1-Cyano-2-phenyl-ethylcarbamoyl)-methyl]-carbamic acid tert-butyl ester

Chemical Property:

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Technology Process of [((S)-1-Cyano-2-phenyl-ethylcarbamoyl)-methyl]-carbamic acid tert-butyl ester

There total 3 articles about [((S)-1-Cyano-2-phenyl-ethylcarbamoyl)-methyl]-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: 91.0%

tert-butyl (S)-N-{2-[(2-amino-1-benzyl-2-oxoethyl)amino]-2-oxoethyl}carbamate (33900-05-9) → [((S)-1-Cyano-2-phenyl-ethylcarbamoyl)-methyl]-carbamic acid tert-butyl ester (99281-91-1)

Guidance literature:

With methoxycarbonylsulfamoyl-triethylammmonium hydroxide; In dichloromethane;

DOI:10.1016/S0040-4039(00)86697-6

Reference yield:

BOC-glycine (4530-20-5) → [((S)-1-Cyano-2-phenyl-ethylcarbamoyl)-methyl]-carbamic acid tert-butyl ester (99281-91-1)

Guidance literature:

Multi-step reaction with 2 steps

1: N-methylmorpholine / tetrahydrofuran / 0.33 h / -15 °C

2: tetrahydrofuran / 2.5 h / -15 - 20 °C

With 4-methyl-morpholine; In tetrahydrofuran;

DOI:10.1021/jm00151a018

Reference yield:

Boc-Gly-OCOOEt (95104-84-0) + L-phenylalanine nitrile methanesulfonate → [((S)-1-Cyano-2-phenyl-ethylcarbamoyl)-methyl]-carbamic acid tert-butyl ester (99281-91-1)

Guidance literature:

In tetrahydrofuran; at -15 - 20 ℃; for 2.5h; Yield given;

DOI:10.1021/jm00151a018

upstream raw materials:

tert-butyl (S)-N-{2-[(2-amino-1-benzyl-2-oxoethyl)amino]-2-oxoethyl}carbamate

Boc-Gly-OCOOEt

BOC-glycine

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