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Water → 2-chloro-4-{[(3S)-1-ethyl-5-oxo-3-pyrrolidinyl]amino}benzonitrile

HRID 1160410
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HRID 1160410 반응식
Cl.[Cl:2][C:3]1[CH:4]=[C:5]([NH:11][C@H:12]([CH2:18][NH:19][CH2:20][CH3:21])[CH2:13][C:14](OC)=[O:15])[CH:6]=[CH:7][C:8]=1[C:9]#[N:10].O.C(=O)(O)[O-].[Na+]>C(OCC)(=O)C>[Cl:2][C:3]1[CH:4]=[C:5]([NH:11][C@H:12]2[CH2:13][C:14](=[O:15])[N:19]([CH2:20][CH3:21])[CH2:18]2)[CH:6]=[CH:7][C:8]=1[C:9]#[N:10]
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참가 물질

5

반응물 3

HCID 962WaterHCID 516892Sodium BicarbonateHCID 131728380Methyl (3S)-3-[(3-chloro-4-cyanophenyl)amino]-4-(ethylamino)butanoate, hydrochloride

생성물 1

HCID 595161932-chloro-4-{[(3S)-1-ethyl-5-oxo-3-pyrrolidinyl]amino}benzonitrile수율 84.3%

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

실험 절차

Methyl (3S)-3-[(3-chloro-4-cyanophenyl)amino]-4-(ethylamino)butanoate, hydrochloride (4.0 g., 13.5 mmole) was redissolved in ethyl acetate (50 mL). Water was added (50 mL) and 10% sodium bicarbonate was added with stirring to bring the pH to 8.5. The organic layer was concentrated and redissolved in benzene (120 mL). The solution was heated with stirring at 75° C. for 6 h. The solvent was evaporated. The crude product was triturated with Et2O, chilled and the solid filtered to give the titled compound (3.0 g, 84%). LC-MS (ES) m/e 263 (M+H)+.

후처리

  1. additionwas added
  2. concentrationThe organic layer was concentrated
  3. dissolutionredissolved in benzene (120 mL)
  4. temperatureThe solution was heated
  5. stirringwith stirring at 75° C. for 6 h
  6. customThe solvent was evaporated
  7. customThe crude product was triturated with Et2O
  8. temperaturechilled
  9. filtrationthe solid filtered

출처 및 근거

ORD 기록
ord-1256a3ac72324cf88b7fdbf627272a99
출처 데이터셋
uspto-grants-2010_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07816395B2

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