1,2-Dichloroethane → 4-(1-Cyclopropyl-1h-pyrazol-4-ylmethyl)-3'-(4-fluoro-phenyl)-3,4,5,6-tetrahydro-2h-[1,2']bipyrazinyl 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.[CH:20]1([N:23]2[CH:27]=[C:26]([CH:28]=O)[CH:25]=[N:24]2)[CH2:22][CH2:21]1.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].[Cl:44]CCCl>>[ClH:44].[CH:20]1([N:23]2[CH:27]=[C:26]([CH2:28][N:17]3[CH2:16][CH2:15][N:14]([C:9]4[C:8]([C:5]5[CH:6]=[CH:7][C:2]([F:1])=[CH:3][CH:4]=5)=[N:13][CH:12]=[CH:11][N:10]=4)[CH2:19][CH2:18]3)[CH:25]=[N:24]2)[CH2:22][CH2:21]1참가 물질
반응물 4
생성물 1
실험 절차
Dissolve 3′-(4-Fluoro-phenyl)-3,4,5,6-tetrahydro-2H-[1,2′]bipyrazinyl (0.157 g, 0.608 mmol) in DCE (5 mL). Add 1-cyclopropyl-1H-pyrazole-4-carbaldehyde (0.354 g, 2.60 mmol) followed by sodium triacetoxyborohydride (0.193 g, 0.912 mmol) and stir at room temperature for 18 hr. Purify via SCX chromatography, followed by silica gel chromatography (eluting with 100:0 to 0:100 hexanes:ethyl acetate then 10:90 methanol:ethyl acetate), to give the free base of the title compound (16 mg, 7%). Dissolve this free base (0.014 g, 0.038 mmol) in methanol and add a solution of ammonium chloride (0.002 g, 0.038 mmol) in a minimal volume of methanol. Shake for 18 hr. at ambient temperature and concentrate to give the title compound (15 mg, 100%). MS (ES): m/z=379 [M+H]+.
후처리
- customPurify via SCX chromatography
- washeluting with 100:0 to 0:100 hexanes
출처 및 근거
- ORD 기록
- ord-d9fb4863e5d84422b3c314b4781febe2
- 출처 데이터셋
- uspto-grants-2012_06
- 특허 번호
- US08202873B2
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