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Hydrochloric Acid → 4-[(2RS, 3S)-3-amino-4-cyclohexyl-2-hydroxybutyryl]morpholine hydrochloride

HRID 986365
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인쇄 미리보기

반응식

HRID 986365 반응식
C(OC([NH:8][C@@H:9]([CH2:20][CH:21]1[CH2:26][CH2:25][CH2:24][CH2:23][CH2:22]1)[CH:10]([OH:19])[C:11]([N:13]1[CH2:18][CH2:17][O:16][CH2:15][CH2:14]1)=[O:12])=O)(C)(C)C.[ClH:27]>CO>[ClH:27].[NH2:8][C@@H:9]([CH2:20][CH:21]1[CH2:26][CH2:25][CH2:24][CH2:23][CH2:22]1)[CH:10]([OH:19])[C:11]([N:13]1[CH2:14][CH2:15][O:16][CH2:17][CH2:18]1)=[O:12]
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참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 867419274-[(2RS, 3S)-3-(tertbutoxycarbonyl)amino-4-cyclohexyl-2-hydroxybutyryl]morpholine

생성물 1

HCID 867419284-[(2RS, 3S)-3-amino-4-cyclohexyl-2-hydroxybutyryl]morpholine hydrochloride

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a solution of 290 mg of the amide compound in 5 ml of methyl alcohol was added 1.0 ml of a 2N-hydrochloric acid, and the mixture was heated under reflux for 3 hours. The reaction mixture was evaporated under reduced pressure to obtain 206 mg of 4-[(2RS, 3S)-3-amino-4-cyclohexyl-2-hydroxybutyryl]morpholine hydrochloride as a white powder.

후처리

  1. temperaturethe mixture was heated
  2. temperatureunder reflux for 3 hours
  3. customThe reaction mixture was evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-c8ebbfe4a24e4984b6da8a311b1e0fa5
출처 데이터셋
uspto-grants-1987_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04711958

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