Hydrochloric Acid → 3-(Cyclopropyl(2-(4-(2-methyl-1H-imidazol-1-yl)phenylamino)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4-yl)amino)propanenitrile
반응식
[C:1]([CH2:3][CH2:4][N:5]([CH:36]1[CH2:38][CH2:37]1)[C:6]1[C:7]2[CH2:28][N:27](C(OC(C)(C)C)=O)[CH2:26][CH2:25][C:8]=2[N:9]=[C:10]([NH:12][C:13]2[CH:18]=[CH:17][C:16]([N:19]3[CH:23]=[CH:22][N:21]=[C:20]3[CH3:24])=[CH:15][CH:14]=2)[N:11]=1)#[N:2].Cl>CO>[CH:36]1([N:5]([C:6]2[C:7]3[CH2:28][NH:27][CH2:26][CH2:25][C:8]=3[N:9]=[C:10]([NH:12][C:13]3[CH:18]=[CH:17][C:16]([N:19]4[CH:23]=[CH:22][N:21]=[C:20]4[CH3:24])=[CH:15][CH:14]=3)[N:11]=2)[CH2:4][CH2:3][C:1]#[N:2])[CH2:37][CH2:38]1참가 물질
4
반응물 2
생성물 1
시약·촉매·용매 1
반응 조건
- 온도
- 80 °C
실험 절차
tert-Butyl 4-((2-cyanoethyl)(cyclopropyl)amino)-2-(4-(2-methyl-1H-imidazol-1-yl)phenylamino)-7,8-dihydropyrido[4,3-d]pyrimidine-6(5H)-carboxylate (240 mg, 0.47 mmol) was dissolved in methanol (5 mL). Hydrochloric acid (0.014 mL, 0.47 mmol) was added and the reaction mixture was stirred at 80° C. for 1 h. The solvent was evaporated under reduced pressure and the crude 3-(cyclopropyl(2-(4-(2-methyl-1H-imidazol-1-yl)phenylamino)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4-yl)amino)propanenitrile (189 mg, 98%) was used as such in the subsequent step. MS (ES+) m/z 415.0 (M+H)+
후처리
- customThe solvent was evaporated under reduced pressure
출처 및 근거
- ORD 기록
- ord-a4fc1fb688424adf87d7cffe91ebfb2c
- 출처 데이터셋
- uspto-grants-2012_05
- 특허 번호
- US08188101B2
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