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Hydrochloric Acid → (2RS, 3S)-3-amino-4-cyclohexyl-2-hydroxy-N-isobutylbutyramide hydrochloride

HRID 986361
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HRID 986361 반응식
C(OC([NH:8][C@@H:9]([CH2:19][CH:20]1[CH2:25][CH2:24][CH2:23][CH2:22][CH2:21]1)[CH:10]([OH:18])[C:11]([NH:13][CH2:14][CH:15]([CH3:17])[CH3:16])=[O:12])=O)(C)(C)C.[ClH:26]>CO>[ClH:26].[NH2:8][C@@H:9]([CH2:19][CH:20]1[CH2:21][CH2:22][CH2:23][CH2:24][CH2:25]1)[CH:10]([OH:18])[C:11]([NH:13][CH2:14][CH:15]([CH3:16])[CH3:17])=[O:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 86741924(2RS, 3S)-3-(tert-butoxycarbonyl)amino-4-cyclohexyl-2-hydroxy-N-isobutylbutyramide

생성물 1

HCID 14181682(2RS, 3S)-3-amino-4-cyclohexyl-2-hydroxy-N-isobutylbutyramide hydrochloride

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a solution of 590 mg of the amide compound in 10 ml of methyl alcohol was added 3.3 ml of a 2N-hydrochloric acid, and the mixture was heated under reflux for 2 hours. The reaction mixture was evaporated under reduced pressure to obtain 254 mg of (2RS, 3S)-3-amino-4-cyclohexyl-2-hydroxy-N-isobutylbutyramide hydrochloride as a white powder.

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후처리

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

출처 및 근거

ORD 기록
ord-e69f516287d149bd99aca742b55ea53e
출처 데이터셋
uspto-grants-1987_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04711958

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