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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 68535377, 화합물 → HCID 23028125, 화합물

HRID 1946440
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인쇄 미리보기

반응식

HRID 1946440 반응식
[Cl:1][C:2]1[N:3]=[C:4]2[CH:9]=[CH:8][C:7]([CH:10]=[CH:11][CH3:12])=[N:6][N:5]2[C:13]=1[S:14]([N:17]=CN(CC(C)C)CC(C)C)(=[O:16])=[O:15].ClC1N=C2C=CC(C3CC3)=NN2C=1S(N=CN(CC(C)C)CC(C)C)(=O)=O>>[Cl:1][C:2]1[N:3]=[C:4]2[CH:9]=[CH:8][C:7](/[CH:10]=[CH:11]/[CH3:12])=[N:6][N:5]2[C:13]=1[S:14]([NH2:17])(=[O:15])=[O:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 68535377HCID 68535377, 화합물HCID 68535409HCID 68535409, 화합물

생성물 1

HCID 23028125HCID 23028125, 화합물수율 70.1%

실험 절차

The reaction was carried out in the same manner as in Reference Example 12 except that N′-(2-chloro-6-(1-propenyl)imidazo[1,2-b]pyridazin-3-ylsulfonyl)-N,N-diisobutylformamidine as a mixture of E and Z was used in place of N′-(2-chloro-6-cyclopropylimidazo[1,2-b]pyridazin-3-ylsulfonyl)-N,N-diisobutylformamidine. The resulting crystals were purified by silica gel column chromatography (chloroform:methanol=20:1), to give the title compound as white crystals. The yield was 70.1%.

후처리

  1. customThe resulting crystals were purified by silica gel column chromatography (chloroform:methanol=20:1)

출처 및 근거

ORD 기록
ord-6a05740e06224ad6a2ad98940164b452
출처 데이터셋
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08399381B2

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