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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 222062생성일: 2026년 10월 26일

Sodium Iodide → 3-Chloro-4-(thiazol-4-ylmethoxy)-phenylamine hydrochloride

https://huagongshe.com/reaction/222062

반응식

참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물Potassium CarbonateHCID 11430—
반응물NitrofunginHCID 12074—
반응물4-(Chloromethyl)-1,3-thiazole hydrochlorideHCID 2763289—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
용매DichloromethaneHCID 6344—
생성물3-Chloro-4-(thiazol-4-ylmethoxy)-phenylamine hydrochlorideHCID 6731322683%

반응 단계

To a solution of 2-chloro-4-nitrophenol (1.00 g, 5.76 mmol) in acetonitrile (125 mL) were added 4-chloromethylthiazole hydrochloride (1.08 g, 6.34 mmol), Potassium carbonate (2.39 g, 17.29 mmol) and sodium iodide (1.73 g, 11.52 mmol). The reaction mixture was stirred at 60 C overnight. Water (60 mL) and DCM (10 mL) were added. After all solid material dissolved, layers formed were separated. The organic layer was washed with water and brine, dried over Na2SO4 and concentrated down to give the required material as a light yellow solid (1.29 mg, 83%). 1H-NMR (CD2Cl2) δ 8.87 (d, 1H), 8.32 (d, 1H), 8.16 (dd, 1H), 7.54-7.56 (m, 1H), 7.22 (d, 1H), 5.33-5.34 (m, 2H); LCMS RT=3.01 min; [M+H]+=271.0.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08207172B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-407926c603784d78906a5cde6a1da983
출처 메모uspto-grants-2012_06