Pyridine → (2R)-2-[(tert-butoxycarbonyl)amino]propyl dimethylcarbamate

HRID 1257883Notes

Reaction equation

HRID 1257883 reaction equation
[CH3:1][N:2]([CH3:6])[C:3](Cl)=[O:4].[C:7]([O:11][C:12](=[O:18])[NH:13][C@H:14]([CH3:17])[CH2:15][OH:16])([CH3:10])([CH3:9])[CH3:8].N1C=CC=CC=1>CN(C)C1C=CN=CC=1.C(Cl)Cl.CCOC(C)=O>[CH3:1][N:2]([CH3:6])[C:3](=[O:4])[O:16][CH2:15][C@H:14]([NH:13][C:12]([O:11][C:7]([CH3:10])([CH3:8])[CH3:9])=[O:18])[CH3:17]

Participants

7

Reactant 3

HCID 1049PyridineHCID 6598Dimethylcarbamoyl ChlorideHCID 13200309tert-butyl N-((2R)-1-hydroxypropan-2-yl)carbamate

Product 1

HCID 86621510(2R)-2-[(tert-butoxycarbonyl)amino]propyl dimethylcarbamate

Reagents, catalysts & solvents 3

HCID 142844-(Dimethylamino)pyridineCatalystHCID 6344DichloromethaneSolventHCID 8857Ethyl AcetateSolvent

Procedure

N,N-Dimethylcarbamoyl chloride (0.12 mL, 0.0013 mol) was added to a solution of tert-butyl[(1R)-2-hydroxy-1-methylethyl]carbamate (0.150 g, 0.856 mmol), 4-dimethylaminopyridine (0.02 g, 0.2 mmol) and pyridine (0.14 g, 1.7 mmol) in methylene chloride (3.0 mL). The mixture was stirred overnight, diluted with EtOAc and washed with 1N HCl, saturated NaHCO3 and brine. The organic layers were dried over Na2SO4, filtered, and concentrated. The residue was purified by chromatography on silica gel with EtOAc in hexanes (0-30%) to afford the desired product.

Workup

  1. washwashed with 1N HCl, saturated NaHCO3 and brine
  2. dry with materialThe organic layers were dried over Na2SO4
  3. filtrationfiltered
  4. concentrationconcentrated
  5. customThe residue was purified by chromatography on silica gel with EtOAc in hexanes (0-30%)

Sources & evidence

ORD record
ord-e46d2fc187d242dabb83f2bd606f1981
Source dataset
uspto-grants-2013_06
Patent number
US08461330B2

Reaction notes

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