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4-fluoro-1H-indazol-3-amine → HCID 178517097, 화합물

HRID 411678
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HRID 411678 반응식
NC1C=CNN=1.O/[CH:8]=[C:9]1\[C:10](=[O:18])[NH:11][C:12]2[C:17]\1=[CH:16][CH:15]=[CH:14][CH:13]=2.[F:19][C:20]1[CH:28]=[CH:27][CH:26]=[C:25]2[C:21]=1[C:22]([NH2:29])=[N:23][NH:24]2>O1CCCC1>[F:19][C:20]1[CH:28]=[CH:27][CH:26]=[C:25]2[C:21]=1[C:22]([NH:29][CH:8]=[C:9]1[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[NH:11][C:10]1=[O:18])=[N:23][NH:24]2
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참가 물질

5

반응물 3

HCID 8179114-fluoro-1H-indazol-3-amineHCID 178418806HCID 178418806, 화합물HCID 178517101HCID 178517101, 화합물

생성물 1

HCID 178517097HCID 178517097, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

The named compound is prepared by substituting 4-fluoro-1H-indazol-3-ylamine for 3-aminopyrazole in the reaction of Example 1. Specifically, E & Z-3-[(hydroxy)-methylene]-1,3-dihydro-indol-2-one (0.100 gms.) is reacted with 0.2186 gms. of 4-fluoro-1H-indazol-3-ylamine by refluxing in tetrahydrofuran (2.5 mL).

후처리

  1. customThe named compound is prepared
  2. customin the reaction of Example 1

출처 및 근거

ORD 기록
ord-ffdaf8574f084e538a695a417b3cd828
출처 데이터셋
uspto-grants-2003_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06559173B1

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