H-D-ALLO-THR-OME HCL
H-D-ALLO-THR-OME HCL Basic information
- Product Name:
- H-D-ALLO-THR-OME HCL
- Synonyms:
-
- H-D-allo-Threonine Methyl Ester Hydrochloride
- H-D-ALLO-THR-OME HCL
- H-D-allo-Thr-OMe
- D(-)-allo-Threonine Methyl ester HCl
- D-Allothreonine, methylester, hydrochloride (1:1)
- H-D-Allo-Thr-Ome Hydrochloride
- methyl (2R,3R)-2-amino-3-hydroxybutanoate hydrochloride
- methyl (2R,3R)-2-amino-3-hydroxybutanoate
- CAS:
- 60538-18-3
- MF:
- C5H12ClNO3
- MW:
- 169.61
- Mol File:
- 60538-18-3.mol
H-D-ALLO-THR-OME HCL Chemical Properties
- Melting point:
- 95-97 °C
- storage temp.
- Sealed in dry,Room Temperature
H-D-ALLO-THR-OME HCL Usage And Synthesis
Uses
H-D-allo-Threonine Methyl Ester Hydrochloride is used to prepare inhibitors of hepatitis A virus 3C cysteine proteinase.
Synthesis
67-56-1
28954-12-3
39994-75-7
General procedure for the synthesis of L-threonine methyl ester hydrochloride from methanol and (2S,3S)-2-amino-3-hydroxybutanoic acid: a mixture of (2S,3S)-2-amino-3-hydroxybutanoic acid (5.4 g, 24.6 mmol) and 6N HCl (60 mL) was refluxed for 5 hours. After completion of the reaction, it was cooled to room temperature and extracted with ether (3 x 70 mL) to remove the by-product benzoic acid. The aqueous phase was concentrated to dryness under reduced pressure and the residue was dried overnight under high vacuum to give crude allo-L-threonine. Methanol (25 mL) was cooled to 0 °C and thionyl chloride (1.80 mL, 25.2 mmol) was added slowly and dropwise. Crude allo-L-threonine was added to the above prepared HCl methanol solution and the reaction mixture was heated to reflux for 1 hour. After removing the solvent under reduced pressure, another batch of HCl methanol solution prepared by the same method was added and heated and refluxed again for 1 hour. The solvent was finally removed under reduced pressure to give allo-L-threonine methyl ester hydrochloride (4.15 g, 98% overall yield in two steps) as a red solid. The product was identified by 1H NMR (300 MHz, CD3OD): δ1.27 (d, J=6.6 Hz, 3H), 4.03 (d, J=3.3 Hz, 1H), 4.27-4.33 (m, 1H); 13C NMR (75 MHz, CD3OD): δ17.13,58.17,65.11,167.62; MS ( ESI, positive): m/z 134 [M+H]+.
References
[1] Journal of Organic Chemistry, 2002, vol. 67, # 5, p. 1536 - 1547
[2] Helvetica Chimica Acta, 1957, vol. 40, p. 1531,1544
[3] Journal of Organic Chemistry, 1997, vol. 62, # 21, p. 7364 - 7375
[4] Journal of Organic Chemistry, 2003, vol. 68, # 26, p. 10046 - 10057
[5] Journal of the American Chemical Society, 2007, vol. 129, # 18, p. 6017 - 6021
H-D-ALLO-THR-OME HCLSupplier
- Tel
- 010-010-82967028 13522913783
- 2355560935@qq.com
- Tel
- 021-54306202 13764082696
- info@hanhongsci.com
- Tel
- 021-50135380
- shchemsky@sina.com
- Tel
- 18270980682
- mlcheng@sunwaypharm.cn
- Tel
- 4009209199
- sales@9dingchem.com
H-D-ALLO-THR-OME HCL(60538-18-3)Related Product Information
- D-Galactosamine pentaacetate
- D-Lysine hydrochloride
- L-Tyrosine Ethyl Ester Hydrochloride
- D-Leucine methyl ester hydrochloride
- H-D-TYR-OME HCL
- METHYL D-HOMOALANINATE HCL
- (S)-3-Amino-3-phenyl propionic acid methylester HCl
- Methyl 4-aminobutyrate hydrochloride
- D-Ornithine monohydrochloride
- L-Valine methyl ester hydrochloride
- D-allo-Isoleucine Ethyl Ester Hydrochloride
- 2-AMINO-2-METHYL-BUTYRIC ACID METHYL ESTER HYDROCHLORIDE
- D-LYSINE METHYL ESTER DIHYDROCHLORIDE
- ETHYL 4-AMINOBUTYRATE HYDROCHLORIDE
- H-ABU-OME HCL
- H-D-PHE-OBZL P-TOSYLATE
- D-(-)-ALPHA-PHENYLGLYCINE ETHYL ESTER HYDROCHLORIDE
- ETHYL-D-ERYTHRO-SPHINGOSINATE HYDROCHLORIDE