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Acetic Acid → (3-{(r)-3-[(2-Chloro-3-trifluoromethyl-benzyl)-((s)-2-phenyl-propyl)-amino]-butoxy}-phenyl)-acetic acid hydrochloride salt

HRID 902674
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HRID 902674 반응식
C[O:2][C:3](=[O:38])[CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([O:11][CH2:12][CH2:13][C@H:14]([N:16]([CH2:26][C:27]2[CH:32]=[CH:31][CH:30]=[C:29]([C:33]([F:36])([F:35])[F:34])[C:28]=2[Cl:37])[CH2:17][C@H:18]([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[CH3:19])[CH3:15])[CH:6]=1.[Li+].[OH-].CC(O)=O.C(OCC)(=O)C>C1COCC1.O>[ClH:37].[Cl:37][C:28]1[C:29]([C:33]([F:34])([F:35])[F:36])=[CH:30][CH:31]=[CH:32][C:27]=1[CH2:26][N:16]([CH2:17][C@H:18]([C:20]1[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=1)[CH3:19])[C@H:14]([CH3:15])[CH2:13][CH2:12][O:11][C:7]1[CH:6]=[C:5]([CH2:4][C:3]([OH:38])=[O:2])[CH:10]=[CH:9][CH:8]=1
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참가 물질

7

반응물 4

HCID 176Acetic AcidHCID 3939Lithium Hydroxide2회HCID 8857Ethyl AcetateHCID 69252464(3-{(R)-3-[(2-Chloro-3-trifluoromethyl-benzyl)-((S)-2-phenyl-propyl)-amino]-butoxy}-phenyl)-acetic Acid Methyl Ester

생성물 1

HCID 69254319(3-{(r)-3-[(2-Chloro-3-trifluoromethyl-benzyl)-((s)-2-phenyl-propyl)-amino]-butoxy}-phenyl)-acetic acid hydrochloride salt
수율 140.2%

시약·촉매·용매 2

HCID 962Water용매2회HCID 8028Tetrahydrofuran용매

실험 절차

A solution of compound (3-{(R)-3-[(2-Chloro-3-trifluoromethyl-benzyl)-((S)-2-phenyl-propyl)-amino]-butoxy}-phenyl)-acetic acid methyl ester (50 mg, 0.1 mmol) in THF (9 ml) and water (6 ml) was treated with aqueous LiOH (1.0 N, 1.0 ml, 1.0 mmol). After stirring at room temperature for 2 h, additional LiOH (1.0 ml, 1.0 mmol) was added and stirring was continued for 2 h. The reaction was neutralized with AcOH and poured into water and ethyl acetate. The aqueous layer was extracted with EtOAc and the combined organic layers were washed with brine, dried over sodium sulfate and concentrated in vacco. The crude mixture was purified by HPLC (YMC CombiPrep ODS-A, 50×20 mm, 20 mL/min, A: acetonitrile B: water, A: 60 to 100% during 10 min, v detection at 254 nm) to give the free acid of title compound as an oil (40 mg, 75%). MS m/e 534.2 (M+H)+. To a solution of the free amine in diethyl ether was added HCl in diethyl ether (1.0M) to precipitate the HCl salt. The suspension was filtered and dried to give the title compound as a white solid.

후처리

  1. stirringstirring
  2. waitwas continued for 2 h
  3. extractionThe aqueous layer was extracted with EtOAc
  4. washthe combined organic layers were washed with brine
  5. dry with materialdried over sodium sulfate
  6. concentrationconcentrated in vacco
  7. customThe crude mixture was purified by HPLC (YMC CombiPrep ODS-A, 50×20 mm, 20 mL/min
  8. waitA: acetonitrile B: water, A: 60 to 100% during 10 min

출처 및 근거

ORD 기록
ord-1e84e6bd5eda4290b6daadc0f82c7a80
출처 데이터셋
uspto-grants-2008_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07365085B2

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