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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 528531생성일: 2026년 10월 25일

2-Aminothiazole → 4-(2-Chloro-4-(trifluoromethyl)phenyl)-N-(thiazol-2-yl)-3,4-dihydro-2H-benzo[b][1,4]oxazine-7-sulfonamide

https://huagongshe.com/reaction/528531

반응식

참여 물질

역할이름HCID투입량
반응물2-AminothiazoleHCID 2155—
반응물4-(2-chloro-4-(trifluoromethyl)phenyl)-3,4-dihydro-2H-benzo[b][1,4]oxazine-7-sulfonyl chlorideHCID 89761722—
생성물4-(2-Chloro-4-(trifluoromethyl)phenyl)-N-(thiazol-2-yl)-3,4-dihydro-2H-benzo[b][1,4]oxazine-7-sulfonamideHCID 71711760—

반응 단계

4-(2-Chloro-4-(trifluoromethyl)phenyl)-N-(thiazol-2-yl)-3,4-dihydro-2H-benzo[b][1,4]oxazine-7-sulfonamide (EXAMPLE 5) was prepared in the same manner as INTERMEDIATE D, step 3, starting from 4-(2-chloro-4-(trifluoromethyl)phenyl)-3,4-dihydro-2H-benzo[b][1,4]oxazine-7-sulfonyl chloride and using thiazol-2-amine instead of intermediate A. 1H NMR (400 MHz, DMSO-d6) δ ppm 3.73 (br. s., 2 H) 4.36 (t, J=4.45 Hz, 2 H) 6.32 (d, J=8.41 Hz, 1 H) 6.79 (d, J=4.50 Hz, 1 H) 7.14 (dd, J=8.61, 2.15 Hz, 1 H) 7.17-7.26 (m, 2 H) 7.73 (d, J=8.31 Hz, 1 H) 7.81-7.88 (m, 1 H) 8.06 (s, 1 H) 12.58 (br. s., 1 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09346798B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-19fae85b9c9e443e8fc4b7edc15e308a
출처 메모uspto-grants-2016_05