반응식
Cl.C(OCC)(=[O:4])C.[Cl:8][C:9]1[CH:28]=[CH:27][C:12]2[O:13][C:14]3[CH:26]=[CH:25][CH:24]=[CH:23][C:15]=3[C@H:16]3[CH2:20][N:19]([CH3:21])[C:18](=[O:22])[C@@H:17]3[C:11]=2[CH:10]=1>C1(C)C(C)=CC=CC=1>[ClH:8].[Cl:8][C:9]1[CH:28]=[CH:27][C:12]2[O:13][C:14]3[CH:26]=[CH:25][CH:24]=[CH:23][C:15]=3[C@@H:16]([CH2:20][NH:19][CH3:21])[C@H:17]([C:18]([OH:22])=[O:4])[C:11]=2[CH:10]=1참가 물질
반응물 3
생성물 1
시약·촉매·용매 1
반응 조건
- 온도
- 65 °C
실험 절차
HCl (55.5 g) and silica gel (55 g) were suspended in xylene (550 mL). The suspension was heated to reflux for 1 night. The reaction mixture was cooled to 65° C. and ethyl acetate (550 mL) was added. The silica gel was filtered off and washed with ethyl acetate (550 mL). The organic phase was evaporated. The crude product was dissolved in methanol (750 mL). The methanol was partly evaporated upon which crystallization of the product takes place. After cooling to 5° C. for 3 hours, the product was obtained by filtration. This yielded trans-11-chloro-2,3,3a,12b-tetrahydro-2-methyl-1H-dibenz[2,3:6,7]oxepino[4,5-c]pyrrol-1-one (IV) (47.8 g, 86%); mp 150.6° C.; 1H-NMR (400.13 MHz in CDCl3 relative to TMS) δ 3.03 (d, 3H), 4.03 (m,1H), 3.53-3.65 (m, 2H), 3.82 (m,1H), 7.01-7.28 (m, 6H), 7.87 (dd, 1H).
후처리
- temperatureThe suspension was heated
- temperatureto reflux for 1 night
- filtrationThe silica gel was filtered off
- washwashed with ethyl acetate (550 mL)
- customThe organic phase was evaporated
- dissolutionThe crude product was dissolved in methanol (750 mL)
- customThe methanol was partly evaporated upon which crystallization of the product
- temperatureAfter cooling to 5° C. for 3 hours
- customthe product was obtained by filtration
출처 및 근거
- ORD 기록
- ord-875d35f175ca4bb684c8dd0ad74a4d63
- 출처 데이터셋
- uspto-grants-2011_01
- 특허 번호
- US07872147B2
연결된 노트
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