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tert-butyl N-((3-(aminomethyl)phenyl)methyl)carbamate → N-(tert-butoxycarbonyl)-N'-[(5-isoquinolyl)sulfonyl]-1,3-xylylenediamine

HRID 10602
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인쇄 미리보기

반응식

HRID 10602 반응식
Cl.[CH:2]1[C:11]2[CH:10]=[CH:9][CH:8]=[C:7]([S:12](Cl)(=[O:14])=[O:13])[C:6]=2[CH:5]=[CH:4][N:3]=1.[C:16]([O:20][C:21]([NH:23][CH2:24][C:25]1[CH:26]=[C:27]([CH:30]=[CH:31][CH:32]=1)[CH2:28][NH2:29])=[O:22])([CH3:19])([CH3:18])[CH3:17]>>[C:16]([O:20][C:21]([NH:23][CH2:24][C:25]1[CH:32]=[CH:31][CH:30]=[C:27]([CH2:28][NH:29][S:12]([C:7]2[CH:8]=[CH:9][CH:10]=[C:11]3[C:6]=2[CH:5]=[CH:4][N:3]=[CH:2]3)(=[O:14])=[O:13])[CH:26]=1)=[O:22])([CH3:19])([CH3:17])[CH3:18]
참가 물질실험 절차출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 2756043tert-butyl N-((3-(aminomethyl)phenyl)methyl)carbamateHCID 13116932Isoquinoline-5-sulfonyl chloride hydrochloride

생성물 1

HCID 69525002N-(tert-butoxycarbonyl)-N'-[(5-isoquinolyl)sulfonyl]-1,3-xylylenediamine수율 78.1%

실험 절차

According to Reference Example 5, Step B, a reaction was performed by using isoquinoline-5-sulfonyl chloride hydrochloride (9 g) and Intermediate 62 (8 g) to obtain the title compound (11.3 g).

출처 및 근거

ORD 기록
ord-5c0b777ddedc4173bf1e910f3e6f9fd8
출처 데이터셋
uspto-grants-2006_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07094789B2

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