Identification | Back Directory | [Name]
2-Cyclopentene-1-carboxylicacid,4-amino-,methylester,(1S,4R)-(9CI) | [CAS]
138923-03-2 | [Synonyms]
(1S,4R)-Methyl 4-aMinocyclopent-2-enecarboxylate Methyl (1S,4R)-4-Amino-2-Cyclopentene-1-Carboxylate methyl (1S,4R)-4-aminocyclopent-2-ene-1-carboxylate (1S,4R)-2-CYCLOPENTENE-1-CARBOXYLIC ACID, 4-AMINOMETHYL ESTER (1S,4R)-Methyl 4-aMinocyclopent-2-enecarboxylate L-tartrate salt Cis-(1S,4R)-4-aMino-2-Cyclopentene-1-carboxylic acid Methyl ester 2-Cyclopentene-1-carboxylicacid,4-amino-,methylester,(1S,4R)-(9CI) 2-Cyclopentene-1-carboxylic acid, 4-amino-, methyl ester, (1S,4R)- | [Molecular Formula]
C7H11NO2 | [MDL Number]
MFCD16293378 | [MOL File]
138923-03-2.mol | [Molecular Weight]
141.17 |
Chemical Properties | Back Directory | [Boiling point ]
191.9±40.0 °C(Predicted) | [density ]
1.109±0.06 g/cm3(Predicted) | [storage temp. ]
Sealed in dry,2-8°C | [pka]
9.66±0.40(Predicted) |
Hazard Information | Back Directory | [Uses]
Methyl (1S,4R)-4-Amino-2-Cyclopentene-1-Carboxylate is used as organic synthesis intermediate and pharmaceutical intermediate, mainly used in laboratory research and development process and chemical production process. | [Synthesis]
Weigh 50g of the by-product (+)1-amino-4-carboxy-2-cyclopentene extracted by γ-lactam enzymatic resolution and put it in a flask, add 200g of water, and slowly add dropwise at 25~30℃ Sulfuric acid, adjust the pH value of the solution to 1~2, after the dripping is completed, add 0.1g of the racemic catalyst o-phthalaldehyde, then heat to reflux, and react for 10~15h. Concentrate under reduced pressure to no fraction, add 200ml of methanol, 20g of tartaric acid, cool to 10-20°C, filter and wash with methanol. Then add 20g of thionyl chloride and 100ml of methanol to the filter cake, react at 65°C for 8h and concentrate under reduced pressure until there is no fraction. Add 100ml of dichloromethane, stir to dissolve and wash the dichloromethane layer twice with drinking water to obtain (- ) Methyl 1-amino-4-carboxylate-2-cyclopentene in dichloromethane solution, yield 42%.
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Acesys Pharmatech
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18860950986 |
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