Triethylamine → Methyl 2-(6-cyano-5-(2,4-dichlorophenyl)-7-methylimidazo[1,2-a]pyrimidin-2-yl)acetate

HRID 1868484노트

반응식

HRID 1868484 반응식
[C:1]([C:4]1[C:5]([CH3:26])=[N:6][C:7]2[N:8]([CH:18]=[C:19]([CH2:21][C:22]([O:24][CH3:25])=[O:23])[N:20]=2)[C:9]=1[C:10]1[CH:15]=[CH:14][C:13]([Cl:16])=[CH:12][C:11]=1[Cl:17])(=O)[NH2:2].CCN(CC)CC.FC(F)(F)C(OC(=O)C(F)(F)F)=O.[NH4+].[Cl-]>C(Cl)Cl>[C:1]([C:4]1[C:5]([CH3:26])=[N:6][C:7]2[N:8]([CH:18]=[C:19]([CH2:21][C:22]([O:24][CH3:25])=[O:23])[N:20]=2)[C:9]=1[C:10]1[CH:15]=[CH:14][C:13]([Cl:16])=[CH:12][C:11]=1[Cl:17])#[N:2]

참가 물질

6

실험 절차

To a suspension of methyl 2-(6-carbamoyl-5-(2,4-dichlorophenyl)-7-methylimidazo[1,2-a]pyrimidin-2-yl)acetate (766 mg, 1.95 mmol) in CH2Cl2 (20 mL) was added Et3N (592 mg, 5.85 mmol) and trifluoroacetic anhydride (819 mg, 3.90 mmol). The reaction mixture became a dark brown-green solution within 2 min. Satd aq NH4Cl (20 mL) was added after 30 min. The organic layer was washed with 20 mL each of satd aq NaHCO3 and water, followed by drying with MgSO4, filtration, and concentration under reduced pressure. The residue was purified by silica gel chromatography eluting product through a 40 mm i.d. by 150 mm column with 1.5% MeOH in CH2Cl2. Concentration of the fractions containing product gave methyl 2-(6-cyano-5-(2,4-dichlorophenyl)-7-methylimidazo[1,2-a]pyrimidin-2-yl)acetate (583 mg, 80%) as a yellow foam.

후처리

  1. customwithin 2 min
  2. washThe organic layer was washed with 20 mL each of satd aq NaHCO3 and water
  3. dry with materialby drying with MgSO4, filtration, and concentration under reduced pressure
  4. customThe residue was purified by silica gel chromatography
  5. washeluting product through a 40 mm i.d
  6. additionConcentration of the fractions containing product

출처 및 근거

ORD 기록
ord-5bdc80f7e0aa423cbf7b510b55469bd0
출처 데이터셋
uspto-grants-2009_12
특허 번호
US07635699B2

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