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(1S, 3R, 4R) -3- (Boc-aMino) -4-этилэфир гидроксициклогексанкарбоновой кислоты

(1S, 3R, 4R) -3- (Boc-aMino) -4-этилэфир гидроксициклогексанкарбоновой кислоты структура
365997-33-7
CAS №
365997-33-7
Химическое название:
(1S, 3R, 4R) -3- (Boc-aMino) -4-этилэфир гидроксициклогексанкарбоновой кислоты
английское имя:
(1S,3R,4R)-3-(Boc-aMino)-4-hydroxy-cyclohexanecarboxylic acid ethyl ester
Синонимы:
Cyclohexanecarboxylic acid,3-[[(1,1-dimethylethoxy)carbonyl]...;(1S,3R,4R)-3-(Boc-aMino)-4-hydroxy-cyclohexanecarboxylic acid ethyl ester;Ethyl (1S,3R,4R)-3-(tert-butoxycarbonylamino)-4-hydroxycyclohexane-1-carboxylate;TIANFU CHEM-- (1S,3R,4R)-3-(Boc-aMino)-4-hydroxy-cyclohexanecarboxylic acid ethyl ester;(1S,3R,4R)-(+)-3-[(tert-Butoxycarbonyl)amino]-4-hydroxycyclohexanecarboxylic acid ethyl ester;Cyclohexanecarboxylic acid,3-[[(1,1-dimethylethoxy)carbonyl]amino]-4-hydroxy-, ethyl ester,(1S,3R,4R)-
CBNumber:
CB02703877
Формула:
C14H25NO5
молекулярный вес:
287.35
MOL File:
365997-33-7.mol

(1S, 3R, 4R) -3- (Boc-aMino) -4-этилэфир гидроксициклогексанкарбоновой кислоты атрибут

Температура плавления: 93-95°C
Температура кипения: 406.6±45.0 °C(Predicted)
плотность: 1.12±0.1 g/cm3(Predicted)
температура хранения: Refrigerator
растворимость: Хлороформ (Мало растворим), ДМСО (Мало растворим), этилацетат (Мало растворим)
форма: Твердый
пка: 11.73±0.60(Predicted)
цвет: От белого до не совсем белого

Заявления о рисках и безопасности

(1S, 3R, 4R) -3- (Boc-aMino) -4-этилэфир гидроксициклогексанкарбоновой кислоты химические свойства, назначение, производство

Использование

(1S,3R,4R)-3-(Boc-aMino)-4-hydroxy-cyclohexanecarboxylic acid ethyl ester, is a building block used in various chemicla synthesis. It can be used for the preparation of six stereoisomers of diaminocyclohexane carboxamide as key intermediates for synthesis of factor Xa inhibitors.

Подготовка

Under 45°C, aqueous ammonia(175 mL) was added to the   (1S,3S,6R)-7-oxabicyclo[4.1.0]heptane-3-carboxylate ethyl (17g, 0.1mmol). After TLC confirmed that the reaction was completed, the reaction liquid was vacuum concentrated. Then 175 mL ethanol was added to the reaction. At room temperature, di-tert-butyl dicarbonate (44.0g, 201mmol) dissolved in ethanol would be added to the above mixture. After reaction for 1h, the solid was concentrated in vacuo, and water (300 mL) was added to the mixture.The water layer was extracted with ethanol (300 mL) twice. The organic phase was collected and dried with anhydrous sodium sulfate. After vacuum concentration, the residue was purified by column chromatography on silica gel to obtain (1S,3R,4R)-3-(Boc-aMino)-4-hydroxy-cyclohexanecarboxylic acid ethyl ester.
(1S,3R,4R)-3-(Boc-aMino)-4-hydroxy-cyclohexanecarboxylic acid ethyl ester

(1S, 3R, 4R) -3- (Boc-aMino) -4-этилэфир гидроксициклогексанкарбоновой кислоты препаратная продукция и сырье

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