(R)-2-[((R)-3-Benzyloxycarbonylamino-3-methoxycarbonyl-propyl)-hydroxy-phosphinoylmethyl]-6-tert-butoxycarbonylamino-heptanedioic acid dimethyl ester

Base Information

Chemical Name:(R)-2-[((R)-3-Benzyloxycarbonylamino-3-methoxycarbonyl-propyl)-hydroxy-phosphinoylmethyl]-6-tert-butoxycarbonylamino-heptanedioic acid dimethyl ester
CAS No.:219752-76-8
Molecular Formula:C₂₈H₄₃N₂O₁₂P
Molecular Weight:630.629
Hs Code.:

(R)-2-[((R)-3-Benzyloxycarbonylamino-3-methoxycarbonyl-propyl)-hydroxy-phosphinoylmethyl]-6-tert-butoxycarbonylamino-heptanedioic acid dimethyl ester

Synonyms:(R)-2-[((R)-3-Benzyloxycarbonylamino-3-methoxycarbonyl-propyl)-hydroxy-phosphinoylmethyl]-6-tert-butoxycarbonylamino-heptanedioic acid dimethyl ester

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Chemical Property of (R)-2-[((R)-3-Benzyloxycarbonylamino-3-methoxycarbonyl-propyl)-hydroxy-phosphinoylmethyl]-6-tert-butoxycarbonylamino-heptanedioic acid dimethyl ester

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Technology Process of (R)-2-[((R)-3-Benzyloxycarbonylamino-3-methoxycarbonyl-propyl)-hydroxy-phosphinoylmethyl]-6-tert-butoxycarbonylamino-heptanedioic acid dimethyl ester

There total 2 articles about (R)-2-[((R)-3-Benzyloxycarbonylamino-3-methoxycarbonyl-propyl)-hydroxy-phosphinoylmethyl]-6-tert-butoxycarbonylamino-heptanedioic acid dimethyl 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: 69.0%

: <(3R)-<3-(benzyloxycarbonyl)amino>-3-carbomethoxypropyl>phosphinate N,N-diisopropylethylamine salt

: 18107-18-1
diazomethyl-trimethyl-silane

: 219752-76-8
(R)-2-[((R)-3-Benzyloxycarbonylamino-3-methoxycarbonyl-propyl)-hydroxy-phosphinoylmethyl]-6-tert-butoxycarbonylamino-heptanedioic acid dimethyl ester

Guidance literature:: With N,O-bis-(trimethylsilyl)-acetamide; In dichloromethane; for 20h; Ambient temperature;
DOI:10.1021/jo981895p

Reference yield:

: methyl (2R)-<(benzyloxycarbonyl)amino>-4-iodobutyrate

: 219752-76-8
(R)-2-[((R)-3-Benzyloxycarbonylamino-3-methoxycarbonyl-propyl)-hydroxy-phosphinoylmethyl]-6-tert-butoxycarbonylamino-heptanedioic acid dimethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 32 percent / ammonium phosphinate, trimethylsilyl chloride / CH₂Cl₂ / Ambient temperature; 1) 3 h, 2) 20 h

2: 69 percent / N,O-bis(trimethylsilyl)acetamide / CH₂Cl₂ / 20 h / Ambient temperature

With chloro-trimethyl-silane; N,O-bis-(trimethylsilyl)-acetamide; ammonium hypophosphite; In dichloromethane;
DOI:10.1021/jo981895p