(R)-(S)-2-benzamido-3-phenylpropyl 2-(tert-butoxycarbonylamino)-3-phenylpropanoate

Base Information

Chemical Name:(R)-(S)-2-benzamido-3-phenylpropyl 2-(tert-butoxycarbonylamino)-3-phenylpropanoate
CAS No.:1042715-31-0
Molecular Formula:C₃₀H₃₄N₂O₅
Molecular Weight:502.61
Hs Code.:

Synonyms:(R)-(S)-2-benzamido-3-phenylpropyl 2-(tert-butoxycarbonylamino)-3-phenylpropanoate

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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 (R)-(S)-2-benzamido-3-phenylpropyl 2-(tert-butoxycarbonylamino)-3-phenylpropanoate

Chemical Property:

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Technology Process of (R)-(S)-2-benzamido-3-phenylpropyl 2-(tert-butoxycarbonylamino)-3-phenylpropanoate

There total 4 articles about (R)-(S)-2-benzamido-3-phenylpropyl 2-(tert-butoxycarbonylamino)-3-phenylpropanoate 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: 65.5%

: 5267-65-2,41072-96-2,92265-06-0,4503-96-2
(S)-N-(1-hydroxy-3-phenylpropan-2-yl)benzamide

: 18942-49-9
Boc-D-Phe-OH

: 1042715-31-0
(R)-(S)-2-benzamido-3-phenylpropyl 2-(tert-butoxycarbonylamino)-3-phenylpropanoate

Guidance literature:: With 1,1'-carbonyldiimidazole; In chloroform; at 20 ℃;
DOI:10.1016/j.ejmech.2016.01.020

Reference yield:

: 3182-95-4
L-Phenylalaninol

: 1042715-31-0
(R)-(S)-2-benzamido-3-phenylpropyl 2-(tert-butoxycarbonylamino)-3-phenylpropanoate

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / methanol / 20 °C

2: 1,1'-carbonyldiimidazole / chloroform / 20 °C

With potassium carbonate; 1,1'-carbonyldiimidazole; In methanol; chloroform;
DOI:10.1016/j.bmcl.2012.01.101

Reference yield:

: 63-91-2,25191-15-5,658-69-5,67675-33-6
L-phenylalanine

: 1042715-31-0
(R)-(S)-2-benzamido-3-phenylpropyl 2-(tert-butoxycarbonylamino)-3-phenylpropanoate

Guidance literature:: Multi-step reaction with 3 steps

1: sodium tetrahydroborate; sulfuric acid; iodine / tetrahydrofuran / Reflux

2: potassium carbonate / methanol / 20 °C

3: 1,1'-carbonyldiimidazole / chloroform / 20 °C

With sodium tetrahydroborate; sulfuric acid; iodine; potassium carbonate; 1,1'-carbonyldiimidazole; In tetrahydrofuran; methanol; chloroform;
DOI:10.1016/j.bmcl.2012.01.101