Dimethylformamide → HCID 58951429, 화합물

HRID 1445755노트

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HRID 1445755 반응식
[CH3:1][S:2]([C:5]1[CH:10]=[CH:9][C:8]([C:11]2[N:16]=[CH:15][C:14]([C:17]3[O:18][C:19]([CH3:26])=[C:20]([CH2:22][C:23]([O-])=[O:24])[N:21]=3)=[CH:13][CH:12]=2)=[CH:7][CH:6]=1)(=[O:4])=[O:3].[Na+].[C:28](Cl)(=O)C(Cl)=O.CN(C)C=O.C[N:40]1[CH2:45][CH2:44]O[CH2:42][CH2:41]1>O1CCOCC1.ClCCl>[CH3:1][S:2]([C:5]1[CH:10]=[CH:9][C:8]([C:11]2[N:16]=[CH:15][C:14]([C:17]3[O:18][C:19]([CH3:26])=[C:20]([CH2:22][C:23]([N:40]4[CH2:41][CH2:42][CH2:28][C@H:45]4[CH3:44])=[O:24])[N:21]=3)=[CH:13][CH:12]=2)=[CH:7][CH:6]=1)(=[O:3])=[O:4]

참가 물질

7

실험 절차

To a stirring solution of Sodium {2-[6-(4-methanesulfonyl-phenyl)-pyridin-3-yl]-5-methyl-oxazol-4-yl}-acetate (See Intermediate 20) (1.0 mmol) and oxalyl chloride (3.0 mmol) in dioxane (0.10M), add a catalytic amount of dimethylformamide and heat to reflux for 30 minutes. After this time, remove the heat and concentrate in vacuo. Take the resulting solid into dichloromethane (0.10M) and slowly add a solution of (R)-methyl-pyrrolidine hydrochloride (1.0 mmol) and n-methylmorpholine (2.0 mmol) in dichloromethane. Stir at room temperature for 1 hour. After this time, the reaction appears complete. Wash the reaction with 1N hydrochloric acid while extracting with dichloromethane. Concentrate the organic layer in vacuo and purify via radial chromatography eluting with methanol and dichloromethane. MS (m/e): 440.2(M+1)

후처리

  1. temperatureheat
  2. temperatureto reflux for 30 minutes
  3. customAfter this time, remove the
  4. temperatureheat
  5. concentrationconcentrate in vacuo
  6. washWash
  7. customthe reaction with 1N hydrochloric acid
  8. extractionwhile extracting with dichloromethane
  9. concentrationConcentrate the organic layer in vacuo
  10. custompurify via radial chromatography
  11. washeluting with methanol and dichloromethane

출처 및 근거

ORD 기록
ord-0fe51d26929a4bb588d1a1c741c6a049
출처 데이터셋
uspto-grants-2010_02
특허 번호
US07666871B2

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