Trifluoroacetic acid → 5,6-Dihydrophenanthridine

HRID 2181844노트

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HRID 2181844 반응식
[Br:1][C:2]1[CH:15]=[CH:14][C:13]2[C:4](=[C:5]3[C:10](=[C:11]([CH2:16][CH3:17])[N:12]=2)[CH:9]=[C:8]([F:18])[CH:7]=[CH:6]3)[CH:3]=1.[BH4-].[Na+].FC(F)(F)C(O)=O.C1C=CC2C3C=CC=CC=3NCC=2C=1.C(N(CC)CC)C.[CH3:49][O:50][C:51]1[CH:56]=[CH:55][C:54]([S:57](Cl)(=[O:59])=[O:58])=[CH:53][CH:52]=1>O1CCCC1.ClCCl>[CH:8]1[CH:7]=[CH:6][C:5]2[C:4]3[CH:3]=[CH:2][CH:15]=[CH:14][C:13]=3[NH:12][CH2:11][C:10]=2[CH:9]=1.[Br:1][C:2]1[CH:15]=[CH:14][C:13]2[N:12]([S:57]([C:54]3[CH:53]=[CH:52][C:51]([O:50][CH3:49])=[CH:56][CH:55]=3)(=[O:59])=[O:58])[CH:11]([CH2:16][CH3:17])[C:10]3[C:5](=[CH:6][CH:7]=[C:8]([F:18])[CH:9]=3)[C:4]=2[CH:3]=1

참가 물질

10

실험 절차

The intermediate dihydrophenanthridine was prepared from 2-bromo-6-ethyl-8-fluorophenanthridine (3.27 g, 10.8 mmol) by treatment with sodium borohydride (2.03 g, 53.8 mmol) and trifluoroacetic acid (3.31 mL, 43.0 mmol) in tetrahydrofuran (43 mL). In a separate, second step, the dihydrophenanthridine was treated with triethylamine (9.0 mL, 65 mmol) and 4-methoxybenzenesulfonyl chloride (2.44 g, 11.8 mmol) in dichloromethane (11 mL) according to the procedure and in the same manner as described in Example 32, Method A, Step d. The crude product was purified by flash column chromatography on silica gel, eluting with a mixture of ethyl acetate-hexane (1:9 to 1:4 gradient), to afford 2-bromo-6-ethyl-8-fluoro-5-[(4-methoxyphenyl)sulfonyl]-5,6-dihydrophenanthridine as a homogeneous, yellow, crystalline, solid, m.p. 133-136° C.;

후처리

  1. customThe crude product was purified by flash column chromatography on silica gel
  2. washeluting with a mixture of ethyl acetate-hexane (1:9 to 1:4 gradient)

출처 및 근거

ORD 기록
ord-931871b17bf045cf984988a113911d7b
출처 데이터셋
uspto-grants-2005_05
특허 번호
US06894061B2

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