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ChemicalBook--->CAS DataBase List--->35150-09-5

35150-09-5

35150-09-5 Structure

35150-09-5 Structure
IdentificationBack Directory
[Name]

BOC-GLY-NH2
[CAS]

35150-09-5
[Synonyms]

BOC-GLY-NH2
Boc-Glycinamide
Boc-glycine amide
N-Boc-glycinamide,95%
N-Boc-glycinaMide, 95%
(Tert-Butoxy)Carbonyl Gly-NH2
TERT-BUTYL CARBAMOYLMETHYLCARBAMATE
N-tert-Butoxycarbonyl-L-glycinamide
TERT-BUTYL 2-AMINO-2-OXOETHYLCARBAMATE
tert-butyl N-(carbamoylmethyl)carbamate
tert-butyl N-(2-amino-2-oxoethyl)carbamate
Carbamic acid, N-(2-amino-2-oxoethyl)-, 1,1-dimethylethyl ester
[EINECS(EC#)]

1533716-785-6
[Molecular Formula]

C7H14N2O3
[MDL Number]

MFCD08275106
[MOL File]

35150-09-5.mol
[Molecular Weight]

174.2
Chemical PropertiesBack Directory
[Melting point ]

85-87 °C
[Boiling point ]

339.7±25.0 °C(Predicted)
[density ]

1.107±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Store in freezer, under -20°C
[form ]

Solid
[pka]

12.01±0.46(Predicted)
[color ]

White
[InChI]

InChI=1S/C7H14N2O3/c1-7(2,3)12-6(11)9-4-5(8)10/h4H2,1-3H3,(H2,8,10)(H,9,11)
[InChIKey]

RHONTQZNLFIDCQ-UHFFFAOYSA-N
[SMILES]

C(OC(C)(C)C)(=O)NCC(N)=O
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2924297099
Hazard InformationBack Directory
[Uses]

Boc-Glycinamide is a useful synthetic intermediate. It is used to prepare primary amides as selective inhibitors of cathepsin K. It is also used to prepare group A streptococcal vaccine.
[Synthesis]

BOC-Glycine

4530-20-5

BOC-GLY-NH2

35150-09-5

Boc-Gly-OH (1.00 g, 5.70 mmol) was dissolved in anhydrous THF (16.0 mL) under nitrogen protection and cooled to 0°C. To this solution was added DIPEA (1.2 mL, 6.84 mmol) and stirred at 0 °C for 30 min. Subsequently, 2,2,2-trichloroethyl chloroformate (0.94 mL, 6.84 mmol) was quickly added and stirring was continued for 30 minutes. Then, a mixture of pre-formulated aqueous NH3 solution (2.0 mL) with THF (2.0 mL) was added. The reaction mixture was gradually warmed up to room temperature and stirred continuously for 16 hours. Upon completion of the reaction, the mixture was concentrated under reduced pressure and the resulting residue was extracted by partitioning with EtOAc (40 mL) and water (40 mL). The aqueous layer was further extracted with EtOAc (2 x 30 mL), and all organic layers were combined and washed sequentially with saturated aqueous NaHCO3 solution (30 mL), water (30 mL) and brine (30 mL). The organic layer was dried with MgSO4, filtered and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography to afford the target compound glycinamide (798 mg, 80% yield) as a colorless oil.

[References]

[1] Journal of Medicinal Chemistry, 2018, vol. 61, # 3, p. 834 - 864
[2] Tetrahedron, 2018, vol. 74, # 15, p. 1951 - 1956
[3] Tetrahedron Letters, 2005, vol. 46, # 40, p. 6879 - 6882
[4] Bioorganic and Medicinal Chemistry Letters, 2012, vol. 22, # 15, p. 4994 - 4997
[5] Tetrahedron Letters, 2003, vol. 44, # 39, p. 7325 - 7328
Spectrum DetailBack Directory
[Spectrum Detail]

BOC-GLY-NH2(35150-09-5)MS
BOC-GLY-NH2(35150-09-5)1HNMR
BOC-GLY-NH2(35150-09-5)IR1
BOC-GLY-NH2(35150-09-5)IR2
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