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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 178418806, 화합물 → HCID 178488692, 화합물

HRID 892030
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HRID 892030 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.[CH3:19][O:20][C:21]1[CH:22]=[C:23]([C:29]2[C:33]([CH3:34])=[N:32][NH:31][C:30]=2[NH2:35])[CH:24]=[CH:25][C:26]=1[O:27][CH3:28]>O1CCCC1>[CH3:19][O:20][C:21]1[CH:22]=[C:23]([C:29]2[C:33]([CH3:34])=[N:32][NH:31][C:30]=2[NH:35][CH:8]=[C:9]2[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[NH:11][C:10]2=[O:18])[CH:24]=[CH:25][C:26]=1[O:27][CH3:28]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 178418806HCID 178418806, 화합물HCID 178488691HCID 178488691, 화합물HCID 178517101HCID 178517101, 화합물

생성물 1

HCID 178488692HCID 178488692, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

The named compound is prepared by substituting 4-(3,4-dimethoxy-phenyl)-5-methyl-2H-pyrazol-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 0.2085 gms. of 4-(3,4-dimethoxy-phenyl)-5-methyl-2H-pyrazol-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-e7e4015fcb7f49b38d547d695287da2b
출처 데이터셋
uspto-grants-2006_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07005444B2

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