(S)-2-[((R)-1-Benzyloxycarbonylamino-3-methyl-butyl)-methoxy-phosphinoyloxy]-3-phenyl-propionic acid methyl ester

Base Information

Chemical Name:(S)-2-[((R)-1-Benzyloxycarbonylamino-3-methyl-butyl)-methoxy-phosphinoyloxy]-3-phenyl-propionic acid methyl ester
CAS No.:208046-11-1
Molecular Formula:C₂₄H₃₂NO₇P
Molecular Weight:477.494
Hs Code.:

Synonyms:(S)-2-[((R)-1-Benzyloxycarbonylamino-3-methyl-butyl)-methoxy-phosphinoyloxy]-3-phenyl-propionic acid methyl ester

Suppliers and Price of (S)-2-[((R)-1-Benzyloxycarbonylamino-3-methyl-butyl)-methoxy-phosphinoyloxy]-3-phenyl-propionic acid methyl ester

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of (S)-2-[((R)-1-Benzyloxycarbonylamino-3-methyl-butyl)-methoxy-phosphinoyloxy]-3-phenyl-propionic acid methyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (S)-2-[((R)-1-Benzyloxycarbonylamino-3-methyl-butyl)-methoxy-phosphinoyloxy]-3-phenyl-propionic acid methyl ester

There total 6 articles about (S)-2-[((R)-1-Benzyloxycarbonylamino-3-methyl-butyl)-methoxy-phosphinoyloxy]-3-phenyl-propionic acid methyl 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:

: 128948-77-6
<(1R)-1-amino>-3-methylbutyl>phosphonic acid

: 208046-11-1
(S)-2-[((R)-1-Benzyloxycarbonylamino-3-methyl-butyl)-methoxy-phosphinoyloxy]-3-phenyl-propionic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 95 percent / 9 h / 110 °C

2: 95 percent / 2 N NaOH / methanol / 12 h / 21 °C

3: SOCl₂ / CH₂Cl₂ / 4 h

4: Et₃N / CH₂Cl₂

With sodium hydroxide; thionyl chloride; triethylamine; In methanol; dichloromethane;
DOI:10.1021/jo00313a012

Reference yield:

: 128948-78-7
methyl hydrogen ((1R)-1-{N-[(phenylmethoxy)carbonyl]amino}-3-methylbutyl)phosphonate

: 208046-11-1
(S)-2-[((R)-1-Benzyloxycarbonylamino-3-methyl-butyl)-methoxy-phosphinoyloxy]-3-phenyl-propionic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: SOCl₂ / CH₂Cl₂ / 4 h

2: Et₃N / CH₂Cl₂

With thionyl chloride; triethylamine; In dichloromethane;
DOI:10.1021/jo00313a012

Reference yield:

: 88081-77-0
L-Leucine phosphonate

: 208046-11-1
(S)-2-[((R)-1-Benzyloxycarbonylamino-3-methyl-butyl)-methoxy-phosphinoyloxy]-3-phenyl-propionic acid methyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: NaHCO₃, Na₂CO₃, 2 N NaOH / H₂O / Ambient temperature

2: 95 percent / 9 h / 110 °C

3: 95 percent / 2 N NaOH / methanol / 12 h / 21 °C

4: SOCl₂ / CH₂Cl₂ / 4 h

5: Et₃N / CH₂Cl₂

With sodium hydroxide; thionyl chloride; sodium hydrogencarbonate; sodium carbonate; triethylamine; In methanol; dichloromethane; water;
DOI:10.1021/jo00313a012