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Thiazole → HCID 178433123, 화합물

HRID 908181
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HRID 908181 반응식
Cl[C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:9](=O)[CH3:10])=[CH:4][C:3]=1[S:12]([NH:15][CH2:16][CH2:17][OH:18])(=[O:14])=[O:13].S1C=CN=C1.ClC1C=CC(CC(=O)C)=CC=1S(N)(=O)=O.ClC1C=CC(C2SC(NC3C=NC=CN=3)=NC=2C)=CC=1S(N)(=O)=O.[NH:63]1[CH:67]=[CH:66][C:65]([NH:68][C:69]([NH2:71])=[S:70])=[N:64]1>>[OH:18][CH2:17][CH2:16][NH:15][S:12]([C:3]1[CH:2]=[CH:7][CH:6]=[C:5]([C:8]2[S:70][C:69]([NH:68][C:65]3[CH:66]=[CH:67][NH:63][N:64]=3)=[N:71][C:9]=2[CH3:10])[CH:4]=1)(=[O:14])=[O:13]
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참가 물질

6

반응물 5

HCID 9256ThiazoleHCID 673909962-Chloro-N-(2-hydroxy-ethyl)-5-(2-oxo-propyl)-benzenesulfonamideHCID 673923132-Chloro-5-(2-oxo-propyl)-benzenesulfonamideHCID 866062162-Chloro-5-[4-methyl-2-(pyrazin-2-ylamino)-thiazol-5-yl]-benzenesulfonamideHCID 178514162HCID 178514162, 화합물

생성물 1

HCID 178433123
HCID 178433123, 화합물

실험 절차

The titled compound was prepared from N-(2-hydroxy-ethyl)-3-(2-oxo-propyl)-benzenesulfonamide (43b) following the two-step procedure (bromination, thiazole formation) described for the conversion of 2-chloro-5-(2-oxo-propyl)-benzene-sulfonamide (33a) to 2-chloro-5-[4-methyl-2-(pyrazin-2-ylamino)-thiazol-5-yl]-benzenesulfonamide (33c) replacing pyrazin-2-yl-thiourea (1a) in the final step with (1H-pyrazol-3-yl)-thiourea (35a).

출처 및 근거

ORD 기록
ord-81bae09f512e4f77a5242aca15becc2a
출처 데이터셋
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08017608B2

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