Hydrochloric Acid → {9-Chloro-1-[6-methoxy-2-(trifluoromethyl)pyridin-3-yl]-1,2,3,4-tetrahydropyrimido[1,2-a]benzimidazol-6-yl}methanol
반응식
[Cl-].[Ca+2].[Cl-].[BH4-].[Na+].[Cl:6][C:7]1[CH:8]=[CH:9][C:10]([C:32](OC)=[O:33])=[C:11]2[C:15]=1[N:14]=[C:13]1[N:16]([C:20]3[C:21]([C:28]([F:31])([F:30])[F:29])=[N:22][C:23]([O:26][CH3:27])=[CH:24][CH:25]=3)[CH2:17][CH2:18][CH2:19][N:12]21.Cl.[Cl-].[NH4+]>C(O)C.O1CCCC1>[Cl:6][C:7]1[C:15]2[N:14]=[C:13]3[N:16]([C:20]4[C:21]([C:28]([F:30])([F:29])[F:31])=[N:22][C:23]([O:26][CH3:27])=[CH:24][CH:25]=4)[CH2:17][CH2:18][CH2:19][N:12]3[C:11]=2[C:10]([CH2:32][OH:33])=[CH:9][CH:8]=1참가 물질
반응물 5
생성물 1
시약·촉매·용매 2
반응 조건
- 온도
- 0 °C
실험 절차
To a solution of calcium chloride (670 mg, 6.04 mmol) in ethanol (15 mL) was added sodium tetrahydroborate (457 mg, 12.08 mmol) at 0° C. The mixture was stirred at 0° C. for 1 hr. A solution of methyl 9-chloro-1-[6-methoxy-2-(trifluoromethyl)pyridin-3-yl]-1,2,3,4-tetrahydropyrimido[1,2-a]benzimidazole-6-carboxylate (1.33 g, 3.02 mmol) in tetrahydrofuran (15 mL) was added dropwise to the mixture at 0° C. The mixture was stirred at 0° C. for 12 hr. 1N HCl (ca. 9.0 mL) was added to the reaction mixture at 0° C., and the aqueous ammonium chloride was added to the mixture. The solvent was removed in vacuo. The precipitated solid was collected by filtration, washed with water and diisopropyl ether to give the title compound (1.33 g, 3.02 mmol, quant) as a white solid.
후처리
- stirringThe mixture was stirred at 0° C. for 12 hr
- customThe solvent was removed in vacuo
- filtrationThe precipitated solid was collected by filtration
- washwashed with water and diisopropyl ether
출처 및 근거
- ORD 기록
- ord-81a19448926a47eba727a4609e31e431
- 출처 데이터셋
- uspto-grants-2014_12
- 특허 번호
- US08901141B2
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