Maleic Anhydride → 4-(2-Chlorophenyl)-9-methoxy-4,5,6,10c-tetrahydro-1H-furo[3,4-c]carbazole-1,3(3aH)-dione

HRID 11127

반응식

HRID 11127 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH:8]=[CH:9][C:10]1[NH:11][C:12]2[C:17]([CH:18]=1)=[CH:16][C:15]([O:19][CH3:20])=[CH:14][CH:13]=2.[C:21]1(=[O:27])[O:26][C:24](=[O:25])[CH:23]=[CH:22]1>C1(C)C(C)=CC=CC=1>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH:8]1[CH:23]2[C:24](=[O:25])[O:26][C:21](=[O:27])[CH:22]2[C:18]2[C:17]3[CH:16]=[C:15]([O:19][CH3:20])[CH:14]=[CH:13][C:12]=3[NH:11][C:10]=2[CH2:9]1

참가 물질

4

실험 절차

A solution of trans-diene (27) (0.30 g, 1.06 mmol) prepared as described in example 37 and maleic anhydride (0.16 g, 1.59 mmol) in xylene (30 mL) were heated at reflux for 18 hours, before being concentrated in vacuo and chromatographed on silica eluting with ethyl acetatelhexane (1:2). Crystallisation from ethyl acetate/hexane then gave anhydride (286) (0.29 g, 72%) as a pale brown powder, mp 189–191° C. 1H NMR δ (CD3)2SO] 11.16 (br s, 1H), 7.69 (dd, J=7.7, 1.4 Hz, 1H), 7.51 (dd, J=7.7, 1.4 Hz, 1H), 7.43 (ddd, J=7.7, 7.7, 1.4 Hz, 1H), 7.36 (ddd, J=7.7, 7.7, 1.4 Hz, 1H), 7.25 (d, J=8.6 Hz, 1H), 7.15 (d, J=2.4 Hz, 1H), 6.77 (dd, J=8.6, 2.4 Hz, 1H), 4.70 (d, J=7.7 Hz, 1H), 4.47 (dd, J=7.7, 3.5 Hz, 1H), 3.78 (s, 3H), 3.71–3.66 (m, 1H), 3.36 (dd, J=15.9, 13.0 Hz, 1H), 2.99 (dd, J=15.9, 4.1 Hz, 1H). Found: C, 65.85; H, 3.95; N, 3.70. C21H16ClNO4 requires: C, 66.06; H, 4.22; N, 3.67.

후처리

  1. temperaturewere heated
  2. temperatureat reflux for 18 hours
  3. concentrationbefore being concentrated in vacuo
  4. customchromatographed on silica eluting with ethyl acetatelhexane (1:2)
  5. customCrystallisation from ethyl acetate/hexane

출처 및 근거

ORD 기록
ord-18531f62cf63405188edd0bdbe1ede32
출처 데이터셋
uspto-grants-2006_08
특허 번호
US07094798B1

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