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Cyclohexanecarboxaldehyde → 3-Cyclohexyl-7-(2'-fluorophenyl)-1,2,3,4-tetrahydro-1,2,4-benzothiadiazine-1,1-dioxide

HRID 1767627
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반응식

HRID 1767627 반응식
[C:1]([C:3]1[CH:4]=[CH:5][C:6]([NH2:13])=[C:7]([S:9]([NH2:12])(=[O:11])=[O:10])[CH:8]=1)#N.[F:14][C:15]1C=[CH:19][CH:18]=[CH:17][C:16]=1B(O)O.[CH:24]1([CH:30]=O)[CH2:29][CH2:28][CH2:27][CH2:26][CH2:25]1>>[CH:24]1([CH:30]2[NH:13][C:6]3[CH:5]=[CH:4][C:3]([C:1]4[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=4[F:14])=[CH:8][C:7]=3[S:9](=[O:11])(=[O:10])[NH:12]2)[CH2:29][CH2:28][CH2:27][CH2:26][CH2:25]1
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참가 물질

4

반응물 3

HCID 16275CyclohexanecarboxaldehydeHCID 27343542-Fluorophenylboronic acidHCID 223239942-Amino-5-cyanobenzene-1-sulfonamide2회

생성물 1

HCID 223239903-Cyclohexyl-7-(2'-fluorophenyl)-1,2,3,4-tetrahydro-1,2,4-benzothiadiazine-1,1-dioxide

실험 절차

5-Iodo-2-aminobenzenesulfonamide (see compound 37) was transformed by Method H (using 2-fluorophenylboronic acid) and Method G (using cyclohexanecarboxaldehyde). M.p. 249–250° C.

출처 및 근거

ORD 기록
ord-6d3f6c252f1b4c3cad43d09ca21bd063
이 페이지에서참가 물질실험 절차출처 및 근거반응 노트
출처 데이터셋
uspto-grants-2007_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07235548B2

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