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Hydrochloric Acid → HCID 59296084, 화합물

HRID 2233381
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HRID 2233381 반응식
Cl[S:2]([C:5]1[CH:14]=[C:13]2[C:8]([C:9]([C:16]([OH:18])=[O:17])=[CH:10][NH:11][C:12]2=[O:15])=[CH:7][CH:6]=1)(=[O:4])=[O:3].[CH2:19]([CH2:21][NH2:22])[OH:20].Cl>O1CCCC1>[OH:20][CH2:19][CH2:21][NH:22][S:2]([C:5]1[CH:14]=[C:13]2[C:8]([C:9]([C:16]([OH:18])=[O:17])=[CH:10][NH:11][C:12]2=[O:15])=[CH:7][CH:6]=1)(=[O:4])=[O:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 700EthanolamineHCID 59295966HCID 59295966, 화합물

생성물 1

HCID 59296084HCID 59296084, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

7-(Chlorosulfonyl)-1-oxo-1,2-dihydroisoquinoline-4-carboxylic acid (1 g) was added to ethanolamine (3 ml) in tetrahydrofuran (3 ml) and the mixture was stirred for 18 h. Hydrochloric acid was added to acidify the mixture, which was filtered to yield 1,2-dihydro-7-[[(2-hydroxyethyl)amino]sulfonyl]-1-oxo-4 isoquinolinecarboxylic acid as a white solid.

후처리

  1. filtrationwas filtered

출처 및 근거

ORD 기록
ord-ed9055cdd71244e1917487faad8996a7
출처 데이터셋
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07709500B2

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