Hydrochloric Acid → N-{3-[2-(3-amino-1-phenyl-propylamino)-pyrimidin-4-yl]-imidazo[1,2-a]pyrazin-8-yl}-cyclohexane-1,4-diamine
반응식
C(OC(=O)[NH:7][CH:8]1[CH2:13][CH2:12][CH:11]([NH:14][C:15]2[C:16]3[N:17]([C:21]([C:24]4[CH:29]=[CH:28][N:27]=[C:26]([NH:30][CH:31]([C:42]5[CH:47]=[CH:46][CH:45]=[CH:44][CH:43]=5)[CH2:32][CH2:33][NH:34]C(OC(C)(C)C)=O)[N:25]=4)=[CH:22][N:23]=3)[CH:18]=[CH:19][N:20]=2)[CH2:10][CH2:9]1)(C)(C)C.Cl>C(O)C>[NH2:34][CH2:33][CH2:32][CH:31]([NH:30][C:26]1[N:25]=[C:24]([C:21]2[N:17]3[CH:18]=[CH:19][N:20]=[C:15]([NH:14][CH:11]4[CH2:12][CH2:13][CH:8]([NH2:7])[CH2:9][CH2:10]4)[C:16]3=[N:23][CH:22]=2)[CH:29]=[CH:28][N:27]=1)[C:42]1[CH:47]=[CH:46][CH:45]=[CH:44][CH:43]=1참가 물질
반응물 2
생성물 1
시약·촉매·용매 1
실험 절차
To a solution of crude (4-{3-[2-(3-tert-butoxycarbonylamino-1-phenyl-propylamino)-pyrimidin-4-yl]-imidazo[1,2-a]pyrazin-8-ylamino}-cyclohexyl)-carbamic acid tert-butyl ester (110 mg, 0.17 mmol) in ethanol (5 mL) was added concentrated hydrochloric acid (5 mL) slowly. The reaction mixture was stirred at room temperature for 15 hours. The solvent was removed under reduced pressure and then the solid was purified by prep-HPLC. Several drops of concentrated HCl were added to the fractions with product. After sonicating for several minutes, solution was concentrated under reduced pressure to afford N-{3-[2-(3-amino-1-phenyl-propylamino)-pyrimidin-4-yl]-imidazo[1,2-a]pyrazin-8-yl}-cyclohexane-1,4-diamine; hydrochloride. (Yield 27 mg, 16.4%). 1H NMR (300 MHz, CD3OD): δ 8.67 (s, 2H), 8.43 (brs, 1H), 7.57-7.55(m, 3H), 7.44-7.31(m, 4H), 5.38 (s, 1H), 4.08 (brs, 1H), 3.21-3.16(m, 3H), 2.42-2.25(m, 6H), 1.75-1.73(m, 4H).
후처리
- customThe solvent was removed under reduced pressure
- customthe solid was purified by prep-HPLC
- additionSeveral drops of concentrated HCl were added to the fractions with product
- customAfter sonicating for several minutes
- concentrationsolution was concentrated under reduced pressure
출처 및 근거
- ORD 기록
- ord-ba7776b176424a1c8ffede53096af1c4
- 출처 데이터셋
- uspto-grants-2014_03
- 특허 번호
- US08673905B2
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