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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2284569생성일: 2026년 10월 24일

Sodium Carbonate → 5-(2-Chloropyridin-3-yl)benzo[d]thiazole

https://huagongshe.com/ko/reaction/2284569

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물5-BromobenzothiazoleHCID 3610155—
반응물2-Chloropyridine-3-boronic acid pinacol esterHCID 12067060—
반응물6-(2-Chloropyridin-3-yl)benzo[d]thiazoleHCID 86715476—
촉매HCID 178418397HCID 178418397—
용매1,4-DioxaneHCID 31275—
생성물5-(2-Chloropyridin-3-yl)benzo[d]thiazoleHCID 8671547770%

반응 단계

5-(2-chloropyridin-3-yl)benzo[d]thiazole was prepared in the similar manner of 6-(2-chloropyridin-3-yl)benzo[d]thiazole by heating the mixture of 5-bromobenzothiazole (1.0 g, 4.67 mmol), 2-chloro-3-pyridine boronic acid pinacol ester (1.34 g, 5.6 mmol), Pd(PPh3)4 (250 mg, 0.22 mmol) and 2M aq.Na2CO3 (7 mL, 14 mmol) in 1,4-dioxane (50 mL). Upon work-up and purification protocol used in the preparation of 6-(2-chloropyridin-3-yl)benzo[d]thiazole provided 5-(2-chloropyridin-3-yl)benzo[d]thiazole as a white solid (820 mg, 70%). 1H NMR (DMSO-d6): δ 9.46 (s, 1H), 8.45 (dd, 1H, J=2.0 and 4.9 Hz), 8.27 (d, 1H, J=8.5 Hz), 8.17 (app s, 1H), 7.97 (dd, 1H, J=1.7 and 7.6 Hz), 7.58 (d, 1H, J=8.5 Hz), 7.53 (dd, 1H, J=4.7 and 7.6 Hz), LCMS: rt 6.73 min (A), purity 99%, MS (m/e) 247.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09145433B2
출처 데이터셋uspto-grants-2015_09
ORD IDord-7cc91fbc5aa5487aa27b74c61924af06
출처 메모uspto-grants-2015_09