p-Toluenesulfonic acid monohydrate → HCID 71240894, 화합물

HRID 1842733

반응식

HRID 1842733 반응식
Cl[C:2]1[N:7]=[C:6]([C:8]2[C:16]3[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=3)[NH:10][CH:9]=2)[C:5]([Cl:17])=[CH:4][N:3]=1.[F:18][C:19]1[C:25]([N+:26]([O-:28])=[O:27])=[CH:24][C:22]([NH2:23])=[C:21]([O:29][CH3:30])[CH:20]=1.O.C1(C)C=CC(S(O)(=O)=O)=CC=1>CC(O)CCC>[Cl:17][C:5]1[C:6]([C:8]2[C:16]3[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=3)[NH:10][CH:9]=2)=[N:7][C:2]([NH:23][C:22]2[CH:24]=[C:25]([N+:26]([O-:28])=[O:27])[C:19]([F:18])=[CH:20][C:21]=2[O:29][CH3:30])=[N:3][CH:4]=1

참가 물질

5

반응물 3

HCID 521998p-Toluenesulfonic acid monohydrateHCID 566553763-(2,5-Dichloropyrimidin-4-yl)-1H-indole2회HCID 574290724-Fluoro-2-methoxy-5-nitroaniline2회

생성물 1

HCID 71240894HCID 71240894, 화합물

시약·촉매·용매 1

HCID 223862-Pentanol용매

반응 조건

온도
125 °C

실험 절차

A mixture of 3-(2,5-dichloropyrimidin-4-yl)-1H-indole (Intermediate 11, 391 mg, 1.48 mmol), 4-fluoro-2-methoxy-5-nitroaniline (Intermediate 23, 289 mg, 1.55 mmol) and p-toluenesulfonic acid monohydrate (310 mg, 1.63 mmol) in 2-pentanol (25 mL) was heated at 125° C. for 18 h. The mixture was cooled and used in the next step without further purification; m/z: ES+ MH+ 414.12.

후처리

  1. temperatureThe mixture was cooled
  2. customused in the next step without further purification

출처 및 근거

ORD 기록
ord-3ece77d72519469a8bc3c96e1c1af865
출처 데이터셋
uspto-grants-2015_02
특허 번호
US08946235B2

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