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HCID 22048460, 화합물 → HCID 22048470, 화합물

HRID 1830804
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HRID 1830804 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([C:8]2[O:9][N:10]=[C:11]3[CH:16]=[CH:15][C:14]([C:17]([C:19]4[S:20][CH:21]=[C:22]([C:24]5[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=5)[N:23]=4)=[O:18])=[CH:13][C:12]=23)[CH:5]=[CH:6][CH:7]=1>O.C1COCC1>[NH2:10][C:11]1[CH:16]=[CH:15][C:14]([C:17]([C:19]2[S:20][CH:21]=[C:22]([C:24]3[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=3)[N:23]=2)=[O:18])=[CH:13][C:12]=1[C:8](=[O:9])[C:4]1[CH:5]=[CH:6][CH:7]=[C:2]([Cl:1])[CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 22048460HCID 22048460, 화합물

생성물 1

HCID 22048470HCID 22048470, 화합물수율 92.8%

시약·촉매·용매 2

HCID 962Water용매HCID 8028Tetrahydrofuran용매

실험 절차

TiCl3 15% in water (300 ml) was added slowly at room temperature to a mixture of intermediate (15) (0.0656 mol) in THF (500 ml). The mixture was stirred at room temperature overnight, then poured out into ice water, extracted with DCM and washed with K2CO3 10%. The organic layer was separated, dried (MgSO4), filtered and the solvent was evaporated till dryness, yielding 25.5 g (92.7%) of [4-amino-3-(3-chlorobenzoyl)phenyl](4-phenyl-2-thiazolyl)-methanone (intermediate 16).

후처리

  1. extractionextracted with DCM
  2. washwashed with K2CO3 10%
  3. customThe organic layer was separated
  4. dry with materialdried (MgSO4)
  5. filtrationfiltered
  6. customthe solvent was evaporated till dryness

출처 및 근거

ORD 기록
ord-11dc14bbbb2246359f1d675dddbe903d
출처 데이터셋
uspto-grants-2006_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07067531B2

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