(S)-N-[2-(acetyloxy)-3-bromopropyl]acetamide
N-[(2S)oxiranylmethyl]acetamide
Conditions | Yield |
---|---|
With potassium carbonate In methanol; acetonitrile at 0 - 20℃; | 90% |
With potassium carbonate In methanol; acetonitrile at 0 - 20℃; | 90% |
With potassium carbonate In methanol; acetonitrile at 0 - 20℃; | 90% |
With potassium carbonate In methanol; acetonitrile at 0 - 20℃; | 90% |
(S)-N-[2-(acetyloxy)-3-bromopropyl]acetamide
3,5-difluoro-4-[3-(tetrazol-2-yl-pyrrolidin-1-yl)]-phenyl carbamic acid benzyl ester
N-((5S)-3-{3,5-difluoro-4-[3-(tetrazol-2-yl)pyrrolidin-1-yl]-phenyl}-2-oxo-5-oxazolidinylmethyl)acetamide
Conditions | Yield |
---|---|
Stage #1: 3,5-difluoro-4-[3-(tetrazol-2-yl-pyrrolidin-1-yl)]-phenyl carbamic acid benzyl ester With lithium tert-butoxide In tetrahydrofuran; N,N-dimethyl-formamide at 20℃; for 0.5h; Stage #2: (S)-N-[2-(acetyloxy)-3-bromopropyl]acetamide In tetrahydrofuran; methanol; N,N-dimethyl-formamide at 20℃; for 48h; | 86% |
isobutyl 4-(1,1-dioxidothiomorpholin-4-yl)-3,5-difluorophenylcarbamate
(S)-N-[2-(acetyloxy)-3-bromopropyl]acetamide
Conditions | Yield |
---|---|
With lithium tert-butoxide In tetrahydrofuran; methanol; acetonitrile | 83% |
(S)-N-[2-(acetyloxy)-3-bromopropyl]acetamide
3-Fluoro-4-(3-cyanopyrrolidin-1-yl)phenylcarbamic acid benzyl ester
N-{(5S)-3-[3-fluoro-4-(3-cyanopyrrolidin-1-yl)phenyl]-2-oxo-5-oxazolidinylmethyl}acetamide
Conditions | Yield |
---|---|
Stage #1: 3-Fluoro-4-(3-cyanopyrrolidin-1-yl)phenylcarbamic acid benzyl ester With lithium tert-butoxide In tetrahydrofuran; N,N-dimethyl-formamide at 20℃; for 0.5h; Stage #2: (S)-N-[2-(acetyloxy)-3-bromopropyl]acetamide In tetrahydrofuran; methanol; N,N-dimethyl-formamide at 20℃; for 96h; | 63% |
(S)-N-[2-(acetyloxy)-3-bromopropyl]acetamide
benzyl [4-(4-cyano-piperidin-1-yl)-3-fluoro-phenyl]-carbamate
(S)-N-{3-[4-(4-cyano-piperidin-1-yl)-3-fluoro-phenyl]-2-oxo-oxazolidin-5-ylmethyl}-acetamide
Conditions | Yield |
---|---|
Stage #1: benzyl [4-(4-cyano-piperidin-1-yl)-3-fluoro-phenyl]-carbamate With lithium tert-butoxide In methanol; N,N-dimethyl-formamide at 20℃; for 0.5h; Stage #2: (S)-N-[2-(acetyloxy)-3-bromopropyl]acetamide In methanol; N,N-dimethyl-formamide at 20℃; for 48h; Product distribution / selectivity; | 59% |
(S)-N-[2-(acetyloxy)-3-bromopropyl]acetamide
N-[[(5S)-3-[3-fluoro-4-(1-methyl-1H-tetrazol-5-yl)-phenyl]-2-oxo-5-oxazolidinyl]methyl]acetamide
Conditions | Yield |
---|---|
Stage #1: benzyl 3-fluoro-4-(1-methyl-1H-tetrazole-5yl)-phenyl carbamate With lithium tert-butoxide In tetrahydrofuran; N,N-dimethyl-formamide at 20℃; for 0.5h; Stage #2: (S)-N-[2-(acetyloxy)-3-bromopropyl]acetamide In tetrahydrofuran; methanol; N,N-dimethyl-formamide at 20℃; for 96h; Product distribution / selectivity; |
Product Name: (S)-N-(3-Bromo-2-acetoxypropyl)acetamide (CAS NO.474021-97-1)
Molecular Formula: C7H12BrNO3
Molecular Weight: 238.08g/mol
Mol File: 474021-97-1.mol
Boiling point: 387.1 °C at 760 mmHg
Flash Point: 187.9 °C
Density: 1.425 g/cm3
Surface Tension: 39.1 dyne/cm
Enthalpy of Vaporization: 63.61 kJ/mol
Vapour Pressure: 3.38E-06 mmHg at 25°C
(S)-N-(3-Bromo-2-acetoxypropyl)acetamide , its CAS NO. is 474021-97-1, the synonyms are (S)-N-Acetoxy-3-bromo-2-acetoxyproylamine ; (S)-N-Acetoxy-3-bromo-2-acetoxypropylamine .
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