Sodium Carbonate → 6-[1-(3,5-Difluoro-benzyl)-piperidin-4-ylamino]-pyridazine-3-carbonitrile
반응식
Cl[C:2]1[N:7]=[N:6][C:5]([C:8]#[N:9])=[CH:4][CH:3]=1.[F:10][C:11]1[CH:12]=[C:13]([CH:22]=[C:23]([F:25])[CH:24]=1)[CH2:14][N:15]1[CH2:20][CH2:19][CH:18]([NH2:21])[CH2:17][CH2:16]1.C(N(C(C)C)CC)(C)C.C(=O)([O-])[O-].[Na+].[Na+]>C(#N)C.O.ClCCl>[F:10][C:11]1[CH:12]=[C:13]([CH:22]=[C:23]([F:25])[CH:24]=1)[CH2:14][N:15]1[CH2:16][CH2:17][CH:18]([NH:21][C:2]2[N:7]=[N:6][C:5]([C:8]#[N:9])=[CH:4][CH:3]=2)[CH2:19][CH2:20]1참가 물질
반응물 4
생성물 1
시약·촉매·용매 3
반응 조건
- 온도
- 120 °C
실험 절차
A mixture of 6-chloro-pyridazine-3-carbonitrile (D4) (1.74 g, 12.46 mmol), 1-(3,5-difluoro-benzyl)-piperidin-4-ylamine (D5) (2.35 g, 10.386 mmol) and diisopropylethylamine (2.71 ml, 15.58 mmol) in acetonitrile (30 ml) was stirred at 120° C. for 40 min., under microwave irradiation (Milestone MW-oven). Dichloromethane, water and a saturated solution of sodium carbonate were then added. The organic layers were filtered over cotton, evaporated in vacuo and the residue was purified by column chromatography (silica gel; 0-1.5% ammonia in methanol (7 M)/dichloromethane). The desired fractions were collected and evaporated in vacuo. The residue was precipitated in heptane to yield E15 (2.065 g, 60%) as a solid. C17H17F2N5 requires 329. Found 330 (MH+); mp: 187.9° C.
후처리
- filtrationThe organic layers were filtered over cotton
- customevaporated in vacuo
- customthe residue was purified by column chromatography (silica gel; 0-1.5% ammonia in methanol (7 M)/dichloromethane)
- customThe desired fractions were collected
- customevaporated in vacuo
- customThe residue was precipitated in heptane
출처 및 근거
- ORD 기록
- ord-d2137ceb23bf4496bde63be1f388efed
- 출처 데이터셋
- uspto-grants-2013_06
- 특허 번호
- US08466153B2
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