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100927-10-4

100927-10-4 Structure

100927-10-4 Structure
IdentificationBack Directory
[Name]

(R)-1-AMinopropan-2-ylcarbaMic Acid tert-Buty Ester
[CAS]

100927-10-4
[Synonyms]

(R)-2-N-Boc-propane-1,2-diaMine
(R)-2-(Boc-amino)-1-propanamine
R-2-N-BOC-propane-1,2-diamine-HCl
(R)-2-(Boc-aMino)-propanaMine HCl
(R)-tert-butyl 1-aminopropan-2-ylcarbamate
tert-butyl (R)-1-aMinopropan-2-ylcarbaMate
tert-Butyl (R)-1-aMinopropan-2-ylcarbaMate HCl
tert-butyl N-[(2R)-1-aMinopropan-2-yl]carbaMate
tert-butyl N-[(1R)-2-amino-1-methyl-ethyl]carbamate
(R)-1-Aminopropan-2-ylcarbamic Acid tert-Buty Ester
tert-butyl (R)-1-aMinopropan-2-ylcarbaMate hydrochloride
((R)-2-Amino-1-methyl-ethyl)-carbamic acid tert-butyl ester
N-[(1R)-2-Amino-1-methylethyl]carbamic acid tert-butyl ester
Carbamic acid, N-[(1R)-2-amino-1-methylethyl]-, 1,1-dimethylethyl ester
Carbamic acid, [(1R)-2-amino-1-methylethyl]-, 1,1-dimethylethyl ester (9CI)
[Molecular Formula]

C8H18N2O2
[MDL Number]

MFCD11112229
[MOL File]

100927-10-4.mol
[Molecular Weight]

174.24
Chemical PropertiesBack Directory
[Boiling point ]

264℃
[density ]

0.984
[Fp ]

113℃
[storage temp. ]

2-8°C(protect from light)
[pka]

12.19±0.46(Predicted)
[Appearance]

White to off-white Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)Corrosion (GHS05)
GHS07,GHS05
[Signal word ]

Danger
[Hazard statements ]

H318-H335-H315
[Precautionary statements ]

P280-P305+P351+P338-P310-P264-P280-P302+P352-P321-P332+P313-P362
[HS Code ]

2924190090
Hazard InformationBack Directory
[Uses]

(R)-1-Aminopropan-2-ylcarbamic Acid tert-Buty Ester is used as an intermediate in the preparation of potent benzothiophene inhibitors of mitogen activated protein kinase-activated protein kinase 2 (MK 2).
[Synthesis]

1,1-Dimethylethyl N-[(1S)-2-azido-1-methylethyl]carbamate

146610-69-7

(R)-1-AMinopropan-2-ylcarbaMic Acid tert-Buty Ester

100927-10-4

To a stirred solution of tert-butyl (S)-1-azidopropan-2-ylcarbamate (S2-3) (6.0 g, 30 mmol) in ethyl acetate (50.0 mL) was added 10% Pd/C (2.3 g). The reaction mixture was stirred at room temperature under hydrogen atmosphere (1 atm) for 15 hours. Upon completion of the reaction, the mixture was filtered through a diatomaceous earth pad and the diatomaceous earth was washed with ethyl acetate. The filtrate was concentrated under reduced pressure to afford tert-butyl N-[(1R)-2-amino-1-methylethyl]carbamate (S2-4) (4.8 g, 92% yield) as a light yellow solid.1H NMR (400 MHz, DMSO-d6) δ 0.95 (d, J = 6.6 Hz, 3H), 1.36 (s, 9H), 2.49 (m, 2H), 3.32 (m, 1H), 6.49 (br s, 1H).

[References]

[1] Patent: US2016/75720, 2016, A1. Location in patent: Paragraph 0247
Spectrum DetailBack Directory
[Spectrum Detail]

(R)-1-AMinopropan-2-ylcarbaMic Acid tert-Buty Ester(100927-10-4)1HNMR
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