| Identification | Back Directory | [Name]
N-CBZ-CIS-4-HYDROXY-D-PROLINE METHYL ESTER | [CAS]
155075-23-3 | [Synonyms]
Methyl N-Cbz-cis -4-Hydroxy-D-prolinate
N-CBZ-CIS-4-HYDROXY-D-PROLINE METHYL ESTER
(4R)-1-Cbz-4-hydroxy-D-proline methyl ester
N-CBZ-CIS-4-HYDROXY-D-PROLINE METHYL ESTER USP/EP/BP
Methyl (2R,4R)-1-Cbz-4-hydroxypyrrolidine-2-carboxylate
-1-Benzyl 2-methyl 4-hydroxypyrrolidine-1,2-dicarboxylate
(2R,4R)-N-1-(benzyloxycarbonyl)-4-hydroxyproline Methyl ester
(2R,4R)-1-benzyl 2-Methyl 4-hydroxypyrrolidine-1,2-dicarboxylate
1-benzyl 2-methyl (2R,4R)-4-hydroxypyrrolidine-1,2-dicarboxylate
(2R,4R)-4-Hydroxy-1,2-pyrrolidinedicarboxylic acid 2-methyl 1-(phenylmethyl) ester
1,2-Pyrrolidinedicarboxylic acid, 4-hydroxy-, 2-methyl 1-(phenylmethyl) ester, (2R,4R)- | [Molecular Formula]
C14H17NO5 | [MDL Number]
MFCD09954933 | [MOL File]
155075-23-3.mol | [Molecular Weight]
279.29 |
| Chemical Properties | Back Directory | [Boiling point ]
422.8±45.0 °C(Predicted) | [density ]
1.313±0.06 g/cm3(Predicted) | [storage temp. ]
Sealed in dry,Room Temperature | [form ]
Solid | [pka]
14.25±0.40(Predicted) | [color ]
White to off-white | [InChI]
InChI=1S/C14H17NO5/c1-19-13(17)12-7-11(16)8-15(12)14(18)20-9-10-5-3-2-4-6-10/h2-6,11-12,16H,7-9H2,1H3/t11-,12-/m1/s1 | [InChIKey]
VVKAGQHUUDRPOI-VXGBXAGGSA-N | [SMILES]
N1(C(OCC2=CC=CC=C2)=O)C[C@H](O)C[C@@H]1C(OC)=O |
| Hazard Information | Back Directory | [Uses]
1-Benzyl 2-methyl (2R,4R)-4-hydroxypyrrolidine-1,2-dicarboxylate is a proline derivative[1]. | [Synthesis]
General procedure for the synthesis of (4R)-N-CBZ-4-hydroxy-D-proline methyl ester from cis-4-hydroxy-D-proline: to a stirred 4R-hydroxypyrrolidine-2R-carboxylic acid (5.02 g, 38.3 mmol, 1 eq.) and sodium bicarbonate (8.05 g, 95.8 mmol, 2.5 eq.) in water (85 mL) at 23°C was A solution of benzyl chloroformate (6.28 mL, 44.0 mmol, 1.15 eq.) in toluene (20 mL) was added slowly over 15 minutes. After 24 hours of reaction, the organic and aqueous layers were separated, the aqueous layer was extracted with ether (2 x 100 mL), and the organic layers were combined and discarded. Subsequently, the aqueous layer was acidified to pH 2 with concentrated hydrochloric acid and the product was extracted with ethyl acetate (2 x 100 mL). The organic layers were combined, dried over anhydrous sodium sulfate and concentrated in vacuum to give (4R)-N-benzyloxycarbonyl-4-hydroxy-D-proline methyl ester (9.97 g, 100% yield). | [References]
[1] Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1144. DOI:10.1080/10408398.2012.708368 |
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