3-Oxo-azetidine-1-carboxylic acid tert-butyl ester → 3-(3-Oxo-4-pyrimidin-2-yl-piperazin-1-yl)-azetidine-1-carboxylic acid tert-butyl ester

HRID 473593

반응식

HRID 473593 반응식
C(O[C:6]([N:8]1[CH2:13][CH2:12][N:11]([C:14]2[N:19]=[CH:18][CH:17]=[CH:16][N:15]=2)[C:10](=[O:20])[CH2:9]1)=O)(C)(C)C.[C:21]([N:28]1[CH2:31]C(=O)[CH2:29]1)([O:23][C:24]([CH3:27])([CH3:26])[CH3:25])=[O:22].[BH-](OC(C)=O)(OC(C)=O)OC(C)=O.[Na+]>C(O)(C(F)(F)F)=O.C(Cl)Cl.ClCCCl.CC(O)=O>[C:24]([O:23][C:21]([N:28]1[CH2:31][CH:6]([N:8]2[CH2:13][CH2:12][N:11]([C:14]3[N:15]=[CH:16][CH:17]=[CH:18][N:19]=3)[C:10](=[O:20])[CH2:9]2)[CH2:29]1)=[O:22])([CH3:27])([CH3:26])[CH3:25]

참가 물질

8

실험 절차

A solution of intermediate 3b (120 mg, 0.43 mmol) in TFA (0.75 mL) and CH2Cl2 (3 mL) was stirred at room temperature for 1.5 h. The solution was concentrated. The resulting residue was stirred with N-Boc-azetidin-3-one 1a (81 mg, 0.47 mmol) and Na(OAc)3BH (100, 0.47 mmol) in 1,2-dichloroethane (4 mL) and HOAc (0.2 mL) at room temperature overnight. The reaction was quenched with aq. NaHCO3. The resulting mixture was extracted with CH2Cl2. The organic solution was dried over Na2SO4 and concentrated. Purification by column chromatography (silica gel, 3% MeOH/CH2Cl2) gave intermediate 3c as light yellow solid (15 mg).

후처리

  1. concentrationThe solution was concentrated
  2. customThe reaction was quenched with aq. NaHCO3
  3. extractionThe resulting mixture was extracted with CH2Cl2
  4. dry with materialThe organic solution was dried over Na2SO4
  5. concentrationconcentrated
  6. customPurification by column chromatography (silica gel, 3% MeOH/CH2Cl2)

출처 및 근거

ORD 기록
ord-e2272eb4ff46483387dd6f0643ba0185
출처 데이터셋
uspto-grants-2014_01
특허 번호
US08637498B2

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