Hydrochloric Acid → 6-(N,N-Dimethylamino-carbonyl)-2,3-dimethyl-8-(trans-1,2,3,4-tetrahydro-2-hydroxy-1-naphthalenyloxy)-imidazo[1,2-a]pyridine hydrochloride
반응식
[CH3:1][N:2]([CH3:17])[C:3]([C:5]1[CH:6]=[C:7]([OH:16])[C:8]2[N:9]([C:11]([CH3:15])=[C:12]([CH3:14])[N:13]=2)[CH:10]=1)=[O:4].[O:18]1[CH:20]2[CH2:21][CH2:22][C:23]3[C:28]([CH:19]12)=[CH:27][CH:26]=[CH:25][CH:24]=3.C(N(CC)CC)C.[ClH:36]>C(O)C.O.C(OCC)(=O)C.C(OCC)C>[ClH:36].[CH3:17][N:2]([CH3:1])[C:3]([C:5]1[CH:6]=[C:7]([O:16][C@@H:19]2[C:28]3[C:23](=[CH:24][CH:25]=[CH:26][CH:27]=3)[CH2:22][CH2:21][C@H:20]2[OH:18])[C:8]2[N:9]([C:11]([CH3:15])=[C:12]([CH3:14])[N:13]=2)[CH:10]=1)=[O:4]참가 물질
반응물 4
생성물 1
시약·촉매·용매 4
실험 절차
To a solution of 1.0 g (4.3 mmol) 6-(N,N-dimethylamino-carbonyl)-8-hydroxy-2,3-dimethyl-imidazo[1,2-a]pyridine in 20 ml ethanol and 5 ml water are added 1.25 g (8.6 mmol) 1,2-epoxy-1,2,3,4-tetrahydro-naphthalene and 1.2 ml triethylamine. After 16 h at 80° C., the mixture is cooled down and partitioned between dichloromethane and saturated aqueous ammonium chloride. The organic layer is separated, dried over anhydrous magnesium sulphate and evaporated. Purification of the residue is achieved by column chromatography on silica gel using ethyl acetate:light petroleum ether (1:1), then dichloro-methane:methanol (20:1). The oil thus obtained is dissolved in ethyl acetate and treated with saturated hydrogen chloride in diethyl ether to give a precipitate which is collected and dried to yield 0.6 g (34%) of the title compound as a colourless solid (m.p. 129° C.).
후처리
- temperaturethe mixture is cooled down
- custompartitioned between dichloromethane and saturated aqueous ammonium chloride
- customThe organic layer is separated
- dry with materialdried over anhydrous magnesium sulphate
- customevaporated
- customPurification of the residue
- customThe oil thus obtained
- customto give a precipitate which
- customis collected
- customdried
출처 및 근거
- ORD 기록
- ord-9747b48df6a445ceb19c6c23901598f3
- 출처 데이터셋
- uspto-grants-2008_02
- 특허 번호
- US07326718B2
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