| Identification | More | [Name]
Z-PHG-OH | [CAS]
53990-33-3 | [Synonyms]
BENZYLOXYCARBONYL-L-PHENYLGLYCINE
CBZ-L-PHENYLGLYCINE
CBZ-PHG-OH
N-ALPHA-CARBOBENZOXY-L-PHENYLGLYCINE
N-ALPHA-CBZ-L-PHENYLGLYCINE
N-CBZ-L-PHENYLGLYCINE
Z-L-PHENYLGLYCINE
Z-PHENYLGLYCINE
Z-(PHENYL)GLY-OH
Z-PHG-OH
Cbz-L-Alpha-Phenylglycine
N-CBZ-L-PHENYLGLYCINE (Z-PHG-OH)
N-CBZ-L-PHENYLGLYCINE(CBZ-PHG-OH)
NALPHA-Benzyloxycarbonyl-L-phenylglycine
BENZYLOXYCARBONYL-L-PHENYLGLYCINE(N-CBZ-L-PHENYLGLYCINE)
Z-L-Phg-OH
N-Carbobenzyloxy-L-phenylglycine | [EINECS(EC#)]
1533716-785-6 | [Molecular Formula]
C16H15NO4 | [MDL Number]
MFCD00077033 | [Molecular Weight]
285.29 | [MOL File]
53990-33-3.mol |
| Chemical Properties | Back Directory | [Melting point ]
131.0 to 135.0 °C | [Boiling point ]
495.3±45.0 °C(Predicted) | [density ]
1.275±0.06 g/cm3(Predicted) | [storage temp. ]
Store at RT. | [solubility ]
DMSO (Slightly), Ethanol (Slightly) | [form ]
Solid | [pka]
3.49±0.10(Predicted) | [color ]
White | [BRN ]
4703006 | [InChI]
InChI=1/C16H15NO4/c18-15(19)14(13-9-5-2-6-10-13)17-16(20)21-11-12-7-3-1-4-8-12/h1-10,14H,11H2,(H,17,20)(H,18,19)/t14-/s3 | [InChIKey]
RLDJWBVOZVJJOS-WDHUHKLTNA-N | [SMILES]
[C@H](C1C=CC=CC=1)(C(=O)O)NC(=O)OCC1C=CC=CC=1 |&1:0,r| | [CAS DataBase Reference]
53990-33-3(CAS DataBase Reference) |
| Hazard Information | Back Directory | [Chemical Properties]
White to off-white powder | [Uses]
Z-L-Phenylglycine is an intermediate for the synthesis of Asimadoline Hydrochlorine (A788250), used in the treatment of IBS, a disorder associated with pain and altered bowel function. | [reaction suitability]
reaction type: solution phase peptide synthesis | [Synthesis]
General procedure for the synthesis of the compound (CAS:5491-18-9) from L-phenylglycine and benzyl chloroformate: To an aqueous solution (500 mL) containing 2-amino-2-phenylacetic acid (20 g, 0.12 mol), sodium carbonate (27.97 g, 0.264 mol) and sodium bicarbonate (11.1 g, 0.132 mol) were added at room temperature. The mixture was stirred until a clarified solution was formed. Acetone (40 mL) was then added and the resulting slightly turbid solution was cooled to 15-20 °C in an ice water bath. Benzyl chloroformate (Cbz-Cl, 28.15 g, 0.165 mol) was added slowly with stirring and then the reaction mixture was gradually warmed to room temperature. After continued stirring for 3 h, the reaction mixture was extracted with methyl tert-butyl ether (100 mL). The pH of the aqueous layer was adjusted with aqueous hydrochloric acid to 2. The oil formed was extracted with ethyl acetate (100 mL x 2). The organic layers were combined, washed with water and concentrated under vacuum to give (S)-2-(((benzyloxy)carbonyl)amino)-2-phenylacetic acid (30.2 g, 80% yield) as a white solid. | [References]
[1] Tetrahedron Letters, 2006, vol. 47, # 36, p. 6393 - 6396
[2] Patent: WO2018/136647, 2018, A2. Location in patent: Page/Page column 29-30
[3] Tetrahedron Letters, 1993, vol. 34, # 39, p. 6329 - 6332
[4] Patent: WO2014/210436, 2014, A2. Location in patent: Paragraph 00520; 00521
[5] Patent: EP1076563, 2005, B1. Location in patent: Page/Page column 9; 13 |
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