돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 70144생성일: 2026년 10월 24일

Hydrochloric Acid → 5-Methyl[1,3]oxazolo[4,5-b]pyridine-2(3H)-thione

https://huagongshe.com/ko/reaction/70144

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Carbon DisulfideHCID 6348—
반응물Potassium HydroxideHCID 14797—
반응물6-Methyl-2-nitropyridin-3-olHCID 84801—
반응물Ammonium formateHCID 2723923—
촉매Palladium hydroxideHCID 9942167—
용매EthanolHCID 702—
생성물5-Methyl[1,3]oxazolo[4,5-b]pyridine-2(3H)-thioneHCID 12664278—

반응 조건

온도70 °C

반응 단계

Ammonium formate (1.64 g, 26 mmol) was added to a suspension of Pd(OH)2 on carbon (˜20% Pd, 0.73 g, 1.0 mmol) and 2-nitro-3-hydroxy-6-methylpyridine (2.0 g, 13 mmol) in EtOH (20 mL). The reaction mixture was heated to 70° C. for 1 h at which point the reaction mixture was allowed to cool to rt and was filtered through Celite®. The filtrate was concentrated under reduced pressure, yielding a thick orangish oil. The material was dissolved in EtOH (25 mL) and potassium hydroxide (0.875 g, 15.6 mmol) and carbon disulfide (15 mL) were added. The reaction mixture was heated to reflux overnight. Upon cooling to rt, the reaction mixture was acidified with 1 N HCl, and the resulting solid was collected by filtration. The solid was washed with water (2×) and air dried followed by drying in a 35° C. vacuum oven. LC-MS: RT=5.58 min, [M+H]+=167.0.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822472B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-64982537af614bce91986c2fc8093296
출처 메모uspto-grants-2014_09