(1S,2R)-2-(N-Benzyloxycarbonyl-N-methyl)amino-1-(tert-butoxycarbonyl)propyl-1-methanesulfonate

Base Information

Chemical Name:(1S,2R)-2-(N-Benzyloxycarbonyl-N-methyl)amino-1-(tert-butoxycarbonyl)propyl-1-methanesulfonate
CAS No.:299926-09-3
Molecular Formula:C₁₈H₂₇NO₇S
Molecular Weight:401.481
Hs Code.:

Synonyms:(1S,2R)-2-(N-Benzyloxycarbonyl-N-methyl)amino-1-(tert-butoxycarbonyl)propyl-1-methanesulfonate

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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 (1S,2R)-2-(N-Benzyloxycarbonyl-N-methyl)amino-1-(tert-butoxycarbonyl)propyl-1-methanesulfonate

Chemical Property:

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Technology Process of (1S,2R)-2-(N-Benzyloxycarbonyl-N-methyl)amino-1-(tert-butoxycarbonyl)propyl-1-methanesulfonate

There total 5 articles about (1S,2R)-2-(N-Benzyloxycarbonyl-N-methyl)amino-1-(tert-butoxycarbonyl)propyl-1-methanesulfonate 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: 100.0%

: 124-63-0
methanesulfonyl chloride

: 299926-07-1
(2S,3R)-tert-Butyl 2-hydroxy-3-(N-benzyloxycarbonyl-N-methyl)aminobutanoate

: 299926-09-3
(1S,2R)-2-(N-Benzyloxycarbonyl-N-methyl)amino-1-(tert-butoxycarbonyl)propyl-1-methanesulfonate

Guidance literature:: With triethylamine; In dichloromethane; at 25 ℃; for 1.5h;
DOI:10.1055/s-2000-6417

Reference yield:

: 79218-15-8
tert-butyl (E)-crotonate

: 299926-09-3
(1S,2R)-2-(N-Benzyloxycarbonyl-N-methyl)amino-1-(tert-butoxycarbonyl)propyl-1-methanesulfonate

Guidance literature:: Multi-step reaction with 5 steps

1.1: 68 percent / (DHQD)2PHAL; aq. K₂OsO₂(OH)4 / acetonitrile

2.1: 96 percent / imidazole / dimethylformamide / 20 h / 25 °C

3.1: NaH / tetrahydrofuran

3.2: 90 percent / tetrahydrofuran / 48 h

4.1: 98 percent / HF / acetonitrile / 1.5 h / 0 - 25 °C

5.1: 100 percent / Et₃N / CH₂Cl₂ / 1.5 h / 25 °C

With 1H-imidazole; potassium dioxotetrahydroxoosmate(VI); hydrogen fluoride; sodium hydride; 1,4-bis(9-O-dihydroquinidine)phthalazine; triethylamine; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; acetonitrile; 1.1: Addition / 2.1: Substitution / 3.1: Metallation / 3.2: Methylation / 4.1: Substitution / 5.1: Substitution;
DOI:10.1055/s-2000-6417

Reference yield:

: 30830-47-8
benzyl N-chlorocarbamate

: 299926-09-3
(1S,2R)-2-(N-Benzyloxycarbonyl-N-methyl)amino-1-(tert-butoxycarbonyl)propyl-1-methanesulfonate

Guidance literature:: Multi-step reaction with 5 steps

1.1: 68 percent / (DHQD)2PHAL; aq. K₂OsO₂(OH)4 / acetonitrile

2.1: 96 percent / imidazole / dimethylformamide / 20 h / 25 °C

3.1: NaH / tetrahydrofuran

3.2: 90 percent / tetrahydrofuran / 48 h

4.1: 98 percent / HF / acetonitrile / 1.5 h / 0 - 25 °C

5.1: 100 percent / Et₃N / CH₂Cl₂ / 1.5 h / 25 °C

With 1H-imidazole; potassium dioxotetrahydroxoosmate(VI); hydrogen fluoride; sodium hydride; 1,4-bis(9-O-dihydroquinidine)phthalazine; triethylamine; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; acetonitrile; 1.1: Addition / 2.1: Substitution / 3.1: Metallation / 3.2: Methylation / 4.1: Substitution / 5.1: Substitution;
DOI:10.1055/s-2000-6417