1,2-Dichloroethane → 4-(3,5-Dimethyl-1-phenyl-1h-pyrazol-4-ylmethyl)-3'-(4-fluorophenyl)-3,4,5,6-tetrahydro-2h-[1,2']bipyrazine hydrochloride
반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[C:9]([N:14]3[CH2:19][CH2:18][NH:17][CH2:16][CH2:15]3)=[N:10][CH:11]=[CH:12][N:13]=2)=[CH:4][CH:3]=1.[CH3:20][C:21]1[C:25]([CH:26]=O)=[C:24]([CH3:28])[N:23]([C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=2)[N:22]=1.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].C(O)(=O)C.[Cl:53]CCCl>>[ClH:53].[CH3:20][C:21]1[C:25]([CH2:26][N:17]2[CH2:16][CH2:15][N:14]([C:9]3[C:8]([C:5]4[CH:6]=[CH:7][C:2]([F:1])=[CH:3][CH:4]=4)=[N:13][CH:12]=[CH:11][N:10]=3)[CH2:19][CH2:18]2)=[C:24]([CH3:28])[N:23]([C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=2)[N:22]=1참가 물질
반응물 5
생성물 1
실험 절차
Dissolve 3′-(4-fluorophenyl)-3,4,5,6-tetrahydro-2H-[1,2′]bipyrazinyl (0.200 g, 0.774 mmol) in DCE (10 mL). Add 3,5-dimethyl-1-phenylpyrazole-4-carboxaldehyde (0.186 g, 0.929 mmol), and stir at room temperature for 10 min. Add sodium triacetoxyborohydride (0.247 g, 1.16 mmol) followed by acetic acid (47 μL, 0.813 mmol). Stir at room temperature for 18 hr. Purify via SCX chromatography, followed by silica gel chromatography, eluting with 0:100 to 10:90 methanol:DCM, followed by reverse phase chromatography to give the free base of the title compound (221 mg, 65%). Dissolve the free base (0.099 g, 0.225 mmol) in methanol and add a solution of ammonium chloride (0.012 g, 0.225 mmol) in a minimal volume of methanol. Shake for 1 hr. at room temperature and concentrate to give the title compound (108 mg, 100%). MS (ES): m/z=443 [M+H]+.
후처리
- customPurify via SCX chromatography
- washeluting with 0:100 to 10:90 methanol
출처 및 근거
- ORD 기록
- ord-37418054f4144a2e946e2439bb2acac6
- 출처 데이터셋
- uspto-grants-2012_06
- 특허 번호
- US08202873B2
반응 노트
불러오는 중…