Water → 3,4,5,6-Tetrahydro-3,10-diaza-benzo[e]azulene-1-carboxylic acid {2-[2-(tetrahydropyran-2-yloxy)-ethoxy]-pyridin-3-yl}amide
반응식
[O:1]1[CH2:6][CH2:5][CH2:4][CH2:3][CH:2]1[O:7][CH2:8][CH2:9][O:10][C:11]1[C:16]([NH2:17])=[CH:15][CH:14]=[CH:13][N:12]=1.C[Al](C)C.C([O:24][C:25]([C:27]1[C:36]2[C:35]3[N:37]=[CH:38][CH:39]=[CH:40][C:34]=3[CH2:33][CH2:32][CH2:31][C:30]=2[NH:29][CH:28]=1)=O)C.O>C(Cl)Cl>[O:1]1[CH2:6][CH2:5][CH2:4][CH2:3][CH:2]1[O:7][CH2:8][CH2:9][O:10][C:11]1[C:16]([NH:17][C:25]([C:27]2[C:36]3[C:35]4[N:37]=[CH:38][CH:39]=[CH:40][C:34]=4[CH2:33][CH2:32][CH2:31][C:30]=3[NH:29][CH:28]=2)=[O:24])=[CH:15][CH:14]=[CH:13][N:12]=1참가 물질
6
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
To a solution of 2-[2-(tetrahydropyran-2-yloxy)-ethoxy]pyridin-3-ylamine (2.3 g, 9.7 mmol) in DCM (8 mL) is added AlMe3 (2M in toluene, 4.9 mL) at rt. After stirring at room temperature for 1 h, a solution of 3,4,5,6-tetrahydro-3,10-diazabenzo[e]azulene-1-carboxylic acid ethyl ester (500 mg, 1.95 mmol) in DCM (10 mL) is added. The mixture is refluxed overnight. On cooling, water (5 mL) is added, and the resulting mixture is extracted with DCM. The combined DCM extracts are dried and solvent removed. The residue is separated by column chromatography on silica gel (5% methanol in DCM) to give 850 mg of 3,4,5,6-tetrahydro-3,10-diaza-benzo[e]azulene-1-carboxylic acid {2-[2-(tetrahydropyran-2-yloxy)-ethoxy]-pyridin-3-yl}amide as an oil.
후처리
- temperatureThe mixture is refluxed overnight
- temperatureOn cooling
- extractionthe resulting mixture is extracted with DCM
- dry with materialThe combined DCM extracts are dried
- customsolvent removed
- customThe residue is separated by column chromatography on silica gel (5% methanol in DCM)
출처 및 근거
- ORD 기록
- ord-526baeee427b494ca58f6b1c9a4d97ff
- 출처 데이터셋
- uspto-grants-2003_11
- 특허 번호
- US06653471B2
반응 노트
불러오는 중…