Hydrochloric Acid → 2-{4-Amino-2-[(3-chloro-4-methoxy-5-methylpyridin-2-yl)methyl]-2,7-dihydro-6-thia-1,2,3,5-tetraazabenzo[cd]azulen-8-yl}-N-methylacetamide hydrochloride

HRID 2093557노트

반응식

HRID 2093557 반응식
Cl.[NH2:2][C:3]1[C:4]2[C:5]3[C:6](=[N:18][N:19]([CH2:21][C:22]4[C:27]([Cl:28])=[C:26]([O:29][CH3:30])[C:25]([CH3:31])=[CH:24][N:23]=4)[N:20]=2)[CH:7]=[C:8]([CH2:13][C:14]([NH:16][CH3:17])=[O:15])[C:9]=3[CH2:10][S:11][N:12]=1>C(O)C>[ClH:28].[NH2:2][C:3]1[C:4]2[C:5]3[C:6](=[N:18][N:19]([CH2:21][C:22]4[C:27]([Cl:28])=[C:26]([O:29][CH3:30])[C:25]([CH3:31])=[CH:24][N:23]=4)[N:20]=2)[CH:7]=[C:8]([CH2:13][C:14]([NH:16][CH3:17])=[O:15])[C:9]=3[CH2:10][S:11][N:12]=1

참가 물질

4

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온도
25 °C

실험 절차

3 N hydrochloric acid (0.786 ml, 2.358 mmol) was added to an ethanol (30 ml) suspension of the above 2-{4-amino-2-[(3-chloro-4-methoxy-5-methylpyridin-2-yl)methyl]-2,7-dihydro-6-thia-1,2,3,5-tetraazabenzo[cd]azulen-8-yl}-N-methylacetamide (527.52 mg, 1.183 mmol), while stirring at 25° C. The resulting mixture was stirred for 1 hour. The precipitated solid was filtered, was washed with ethanol (6 ml), and was then dried under reduced pressure at 40° C. for 30 minutes, so as to obtain the title compound (531.09 mg, 1.101 mmol).

후처리

  1. stirringThe resulting mixture was stirred for 1 hour
  2. filtrationThe precipitated solid was filtered
  3. washwas washed with ethanol (6 ml)
  4. customwas then dried under reduced pressure at 40° C. for 30 minutes

출처 및 근거

ORD 기록
ord-8fad8ee5da22413cbf031c29612a0ba6
출처 데이터셋
uspto-grants-2013_05
특허 번호
US08445504B2

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