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Diisopropylamine → (S)-4,4-difluoro-2-[(morpholine-4-carbonyl)-amino]-5-phenyl-pentanoic acid methyl ester

HRID 1455568
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HRID 1455568 반응식
Cl.[CH3:2][O:3][C:4](=[O:18])[C@@H:5]([NH2:17])[CH2:6][C:7]([F:16])([F:15])[CH2:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1.C(NC(C)C)(C)C.[N:26]1([C:32](Cl)=[O:33])[CH2:31][CH2:30][O:29][CH2:28][CH2:27]1>ClCCl.O>[CH3:2][O:3][C:4](=[O:18])[C@@H:5]([NH:17][C:32]([N:26]1[CH2:31][CH2:30][O:29][CH2:28][CH2:27]1)=[O:33])[CH2:6][C:7]([F:16])([F:15])[CH2:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1
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참가 물질

6

반응물 3

HCID 7912DiisopropylamineHCID 848104-Morpholinecarbonyl chlorideHCID 68820868(S)-2-amino-4,4-difluoro-5-phenyl-pentanoic acid methyl ester hydrochloride

생성물 1

HCID 57535362(S)-4,4-difluoro-2-[(morpholine-4-carbonyl)-amino]-5-phenyl-pentanoic acid methyl ester수율 88.5%

시약·촉매·용매 2

HCID 962Water용매
HCID 6344
Dichloromethane
용매

실험 절차

To a mixture of (S)-2-amino-4,4-difluoro-5-phenyl-pentanoic acid methyl ester hydrochloride (2.50 g, 8.94 mmol) and diisopropyl amine (22.3 mmol, 2.89 g) in dry dichloromethane (40 mL) under N2 is added drop wise morpholine carbonyl chloride (13.4 mmol, 2.0 g). The mixture is stirred at room temperature for 15 hours, and then diluted with water (50 mL). The aqueous layer is extracted with dichloromethane (30 mL). The organic layers are dried over magnesium sulfate and then concentrated in vacuum. Purification over 110 g silica gel, eluting with EtOAc:Heptane (1:1, then 2:1) affords (S)-4,4-difluoro-2-[(morpholine-4-carbonyl)-amino]-5-phenyl-pentanoic acid methyl ester (2.82 g, 88.5%).

후처리

  1. extractionThe aqueous layer is extracted with dichloromethane (30 mL)
  2. dry with materialThe organic layers are dried over magnesium sulfate
  3. concentrationconcentrated in vacuum
  4. customPurification over 110 g silica gel
  5. washeluting with EtOAc:Heptane (1:1

출처 및 근거

ORD 기록
ord-2d5cbf0c018e4446a35ea53c000e8e66
출처 데이터셋
uspto-grants-2009_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07482448B2

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