돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 70142생성일: 2026년 10월 24일

Hydrochloric Acid → 2-Chloro-(1,3)thiazolo(4,5-b)pyridine

https://huagongshe.com/ko/reaction/70142

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물2-Amino-3-bromopyridineHCID 817700—
반응물Potassium ethylxanthateHCID 2735045—
용매DimethylformamideHCID 6228—
생성물2-Chloro-(1,3)thiazolo(4,5-b)pyridineHCID 51358428—

반응 단계

2-Amino-3-bromopyridine (1.0 g, 5.8 mmol) and potassium ethyl xanthate (2.22 g, 13.9 mmol) were heated to 130° C. in DMF (5 mL) overnight. After cooling to rt, the reaction mixture was diluted with 1 M aqueous HCl (30 mL) and stirred at rt for an additional 1 h. The resulting solid was collected by filtration, washed with water (2×), and air-dried. The material was suspended in CH2Cl2 (2 mL) and sulfuryl chloride (5 mL) was added. After 2 h, water (30 mL) was added to decompose the excess sulfuryl chloride. The reaction mixture was diluted with EtOAc (30 mL) and washed with water (2×) and brine. The EtOAc layer was discarded. The combined aqueous washes were brought to pH ˜12 with 1 N aqueous NaOH and were extracted with EtOAc (3×). The combined EtOAc extracts were dried over Na2SO4, filtered, and concentrated under reduced pressure. This gave 0.933 g (95%) of the title compound as a yellow solid. LC-MS: RT=5.81 min., [M+H]+=171.1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822472B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-daa3ea91cf524e27b73f2ed451cffce0
출처 메모uspto-grants-2014_09