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Hydrochloric Acid → (S)-2-Amino-3-(4-(trifluoromethoxy)phenyl)propanoic acid hydrochloride

HRID 1799301
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HRID 1799301 반응식
C([NH:4][C@@H:5]([CH2:10][C:11]1[CH:16]=[CH:15][C:14]([O:17][C:18]([F:21])([F:20])[F:19])=[CH:13][CH:12]=1)[C:6]([O:8]C)=[O:7])(=O)C.[ClH:22]>>[ClH:22].[NH2:4][C@@H:5]([CH2:10][C:11]1[CH:12]=[CH:13][C:14]([O:17][C:18]([F:19])([F:20])[F:21])=[CH:15][CH:16]=1)[C:6]([OH:8])=[O:7]
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참가 물질

3

반응물 2

HCID 313Hydrochloric AcidHCID 22950700Methyl (2s)-2-(acetylamino)-3-[4-(trifluoromethoxy)phenyl]propanoate

생성물 1

HCID 69017088(S)-2-Amino-3-(4-(trifluoromethoxy)phenyl)propanoic acid hydrochloride수율 93%

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온도
100 °C

실험 절차

A 6 N hydrochloric acid (330 μL) solution of methyl (2S)-2-(acetylamino)-3-[4-(trifluoromethoxy)phenyl]propanoate (29.9 mg, 0.098 mmol) prepared in Reference Example 3 (3f) was stirred at 100° C. for 4 hours. The reaction solution was cooled to room temperature and then concentrated under reduced pressure. The obtained residue was azeotroped with toluene, washed with diethyl ether, and dried under reduced pressure to give 26 mg of the title compound (white powder, yield: 93%).

후처리

  1. temperatureThe reaction solution was cooled to room temperature
  2. concentrationconcentrated under reduced pressure
  3. customThe obtained residue was azeotroped with toluene
  4. washwashed with diethyl ether
  5. customdried under reduced pressure

출처 및 근거

ORD 기록
ord-35acec976dbf4a369c114781f4a5801d
출처 데이터셋
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08344029B2

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