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HCID 15158253, 화합물 → HCID 15158254, 화합물

HRID 1646401
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HRID 1646401 반응식
Cl[C:2]1[N:7]=[CH:6][N:5]=[C:4]([NH:8][N:9]2[C:21]3[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=3[C:15]3[C:10]2=[CH:11][CH:12]=[CH:13][CH:14]=3)[CH:3]=1>C(O)C.[Pd]>[N:7]1[CH:2]=[CH:3][C:4]([NH:8][N:9]2[C:21]3[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=3[C:15]3[C:10]2=[CH:11][CH:12]=[CH:13][CH:14]=3)=[N:5][CH:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 15158253HCID 15158253, 화합물

생성물 1

HCID 15158254HCID 15158254, 화합물수율 175.5%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매2회

실험 절차

To a slurry of 10% Pd/C (1.0 g) and 0.8 g MgO in 5 ml of ethanol was added 4.0 g of N-(6-chloropyrimidin-4-yl)-9H-carbazol-9-amine in 12.0 ml of ethanol and the mixture was hydrogenated at atmospheric pressure at room temperature. When the reaction was complete, the mixture was filtered and the filtrate was evaporated to yield 6.2 g of an oil, which was preabsorbed on silica gel and eluted with 5% ethyl acetate/DCM on a silica gel column via the flash method. The desired fractions were evaporated to yield 2.4 g (61.5%) of a solid, N-(pyrimidin-4-yl)-9H-carbazol-9-amine, m.p. 177°-180° C.

후처리

  1. customwas hydrogenated at atmospheric pressure at room temperature
  2. filtrationthe mixture was filtered
  3. customthe filtrate was evaporated

출처 및 근거

ORD 기록
ord-53970b26786f41a7ae7d8175fbe0e81f
출처 데이터셋
uspto-grants-1993_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05179204

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