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Water → 2-(Chloromethyl)-N-[6-(1H-indol-4-yl)-1-(phenylsulfonyl)-1H-indazol-4-yl]-1,3-thiazole-4-carboxamide

HRID 244697
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HRID 244697 반응식
[NH:1]1[C:9]2[C:4](=[C:5]([C:10]3[CH:11]=[C:12]([NH2:28])[C:13]4[CH:14]=[N:15][N:16]([S:19]([C:22]5[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=5)(=[O:21])=[O:20])[C:17]=4[CH:18]=3)[CH:6]=[CH:7][CH:8]=2)[CH:3]=[CH:2]1.CCN(C(C)C)C(C)C.[Cl:38][CH2:39][C:40]1[S:41][CH:42]=[C:43]([C:45](Cl)=[O:46])[N:44]=1.O>C(Cl)(Cl)Cl>[Cl:38][CH2:39][C:40]1[S:41][CH:42]=[C:43]([C:45]([NH:28][C:12]2[CH:11]=[C:10]([C:5]3[CH:6]=[CH:7][CH:8]=[C:9]4[C:4]=3[CH:3]=[CH:2][NH:1]4)[CH:18]=[C:17]3[C:13]=2[CH:14]=[N:15][N:16]3[S:19]([C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)(=[O:21])=[O:20])=[O:46])[N:44]=1
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참가 물질

6

반응물 4

HCID 962WaterHCID 81531DiisopropylethylamineHCID 582680186-(1H-indol-4-yl)-1-(phenylsulfonyl)-1H-indazol-4-amineHCID 597024562-(Chloromethyl)-1,3-thiazole-4-carbonyl chloride2회

생성물 1

HCID 583563582-(Chloromethyl)-N-[6-(1H-indol-4-yl)-1-(phenylsulfonyl)-1H-indazol-4-yl]-1,3-thiazole-4-carboxamide수율 75.6%

시약·촉매·용매

1
HCID 6212Chloroform용매2회

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온도
0 °C

실험 절차

To solution of 6-(1H-indol-4-yl)-1-(phenylsulfonyl)-1H-indazol-4-amine (1.5 g, 3.86 mmol) in chloroform (20 ml) at 0° C. was added DIPEA (1.35 ml, 7.72 mmol). 2-(Chloromethyl)-1,3-thiazole-4-carbonyl chloride (1.8 g, 6.98 mmol) in chloroform (20 ml) was added dropwise and the mixture was stirred at 0° C. for 1 h 15 mins. The mixture was allowed to warm to room temperature and stirring continued for 18 h. A further portion of 2-(chloromethyl)-1,3-thiazole-4-carbonyl chloride (0.2 g, 1.02 mmol) was added to the mixture which was stirred at room temperature for 30 mins. Water (50 ml) was added to quench the reaction and the mixture was extracted with DCM (2×100 ml), separating the layers using a hydrophobic frit. The organics were collected and solvent removed in vacuo to give a brown solid which was triturated with ether (10 ml). The solid was filtered off and dried in a vacuum oven overnight to afford the title compound (1.6 g).

후처리

  1. temperatureto warm to room temperature
  2. stirringstirring
  3. waitcontinued for 18 h
  4. stirringwas stirred at room temperature for 30 mins
  5. customto quench
  6. customthe reaction
  7. extractionthe mixture was extracted with DCM (2×100 ml)
  8. customseparating the layers
  9. customThe organics were collected
  10. customsolvent removed in vacuo
  11. customto give a brown solid which
  12. customwas triturated with ether (10 ml)
  13. filtrationThe solid was filtered off
  14. customdried in a vacuum oven overnight

출처 및 근거

ORD 기록
ord-7284d3b6ef9a4bcbafa4616bbda56ee6
출처 데이터셋
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08658635B2

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