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HCID 12557673, 화합물 → HCID 54712699, 화합물

HRID 1719505
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HRID 1719505 반응식
[OH:1][C:2]1[C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][C:6]=2[S:5](=[O:13])(=[O:12])[N:4]([CH3:14])[C:3]=1[C:15]([O:17]C)=O.[NH2:19][C:20]1[C:21](=[O:28])[CH:22]=[CH:23][C:24]([Cl:27])=[CH:25][CH:26]=1>C1(C)C(C)=CC=CC=1>[Cl:27][C:24]1[CH:23]=[CH:22][C:21](=[O:28])[C:20]([NH:19][C:15]([C:3]2[N:4]([CH3:14])[S:5](=[O:12])(=[O:13])[C:6]3[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=3[C:2]=2[OH:1])=[O:17])=[CH:26][CH:25]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 12557673HCID 12557673, 화합물HCID 54676532methyl 4-hydroxy-2-methyl-2H-1,2-benzothiazine-3-carboxylate 1,1-dioxide

생성물 1

HCID 54712699HCID 54712699, 화합물수율 40.7%

시약·촉매·용매 1

HCID 7237O-Xylene용매

실험 절차

A mixture of methyl 4-hydroxy-2-methyl-2H-1,2-benzothiazine-3-carboxylate 1,1-dioxide (1.5 g) and 2-amino-5-chloro-2,4,6-cycloheptatrien-1-one (0.87 g) in xylene (37 ml) was refluxed for 24 hours. The reaction mixture was cooled to room temperature. The crystals were collected by filtration and recrystallized from N,N-dimethylformamide to give N-(5-chloro-1-oxo-2,4,6-cycloheptatrien-2-yl)-4-hydroxy-2-methyl-2H-1,2-benzothiazine-3-carboxamide 1,1-dioxide (0.89 g).

후처리

  1. temperaturewas refluxed for 24 hours
  2. filtrationThe crystals were collected by filtration
  3. customrecrystallized from N,N-dimethylformamide

출처 및 근거

ORD 기록
ord-a83a937ca36c4318a448c7744e506a25
출처 데이터셋
uspto-grants-1985_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04540692

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