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Sodium Thiosulfate → Ethyl 5-(2-(5-fluoro-2-methoxyphenyl)-4-oxopyrrolidin-1-yl)pyrazolo[1,5-a]pyrimidine-3-carboxylate

HRID 1426987
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HRID 1426987 반응식
CC(OI1(OC(C)=O)(OC(C)=O)OC(=O)C2C=CC=CC1=2)=O.[F:23][C:24]1[CH:25]=[CH:26][C:27]([O:50][CH3:51])=[C:28]([C@H:30]2[CH2:34][CH:33]([OH:35])[CH2:32][N:31]2[C:36]2[CH:41]=[CH:40][N:39]3[N:42]=[CH:43][C:44]([C:45]([O:47][CH2:48][CH3:49])=[O:46])=[C:38]3[N:37]=2)[CH:29]=1.[O-]S([O-])(=S)=O.[Na+].[Na+]>C(Cl)Cl>[F:23][C:24]1[CH:25]=[CH:26][C:27]([O:50][CH3:51])=[C:28]([CH:30]2[CH2:34][C:33](=[O:35])[CH2:32][N:31]2[C:36]2[CH:41]=[CH:40][N:39]3[N:42]=[CH:43][C:44]([C:45]([O:47][CH2:48][CH3:49])=[O:46])=[C:38]3[N:37]=2)[CH:29]=1
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5

반응물 3

HCID 24477Sodium ThiosulfateHCID 159087TriacetoxyperiodinaneHCID 86691712(R)-ethyl 5-(2-(5-fluoro-2-methoxyphenyl)-4-hydroxypyrrolidin-1-yl)pyrazolo[1,5-a]pyrimidine-3-carboxylate

생성물 1

HCID 86691759Ethyl 5-(2-(5-fluoro-2-methoxyphenyl)-4-oxopyrrolidin-1-yl)pyrazolo[1,5-a]pyrimidine-3-carboxylate수율 82.5%

시약·촉매·용매 1

HCID 6344
Dichloromethane
용매
2회

실험 절차

To a suspension of Dess-Martin periodinane (0.233 g, 0.549 mmol) in CH2Cl2 (2.2 mL) at 0° C. was added a solution of (R)-ethyl 5-(2-(5-fluoro-2-methoxyphenyl)-4-hydroxypyrrolidin-1-yl)pyrazolo[1,5-a]pyrimidine-3-carboxylate (0.200 g, 0.499 mmol) in CH2Cl2 (1.5 mL). The resulting mixture was warmed to ambient temperature and stirred for 18 hours. The reaction mixture was cooled to 0° C. and quenched with saturated aqueous NaHCO3 (5 mL) containing Na2S2O3 (0.608 g, 3.85 mmol). The resulting mixture was warmed to ambient temperature and stirred for 10 minutes. The organic layer was separated, washed with saturated aqueous NaHCO3 (10 mL) followed by brine (10 mL), dried over MgSO4, filtered, and concentrated under reduced pressure to afford ethyl 5-(2-(5-fluoro-2-methoxyphenyl)-4-oxopyrrolidin-1-yl)pyrazolo[1,5-a]pyrimidine-3-carboxylate (0.164 g, 82.4% yield). LC/MS (ES+APCI) m/z=399.1 (M+H).

후처리

  1. temperatureThe reaction mixture was cooled to 0° C.
  2. customquenched with saturated aqueous NaHCO3 (5 mL)
  3. temperatureThe resulting mixture was warmed to ambient temperature
  4. stirringstirred for 10 minutes
  5. customThe organic layer was separated
  6. washwashed with saturated aqueous NaHCO3 (10 mL)
  7. dry with materialdried over MgSO4
  8. filtrationfiltered
  9. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-96637b95acf244d184188ae2de2f3a9b
출처 데이터셋
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08933084B2

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