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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 448129생성일: 2026년 10월 25일

Pyridine → HCID 66784763, 화합물

https://huagongshe.com/reaction/448129

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Oxalyl chlorideHCID 65578—
반응물4-(Morpholin-4-yl)benzoic acidHCID 345278—
반응물Sodium BicarbonateHCID 516892—
반응물5-tert-butyl 1-ethyl 3-amino-1H-thieno[2,3-c]pyrazole-1,5-dicarboxylateHCID 57737272—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물HCID 66784763HCID 6678476341.9%

반응 조건

온도5 °C

반응 단계

Oxalyl chloride (20.2 mL, 231 mmol) was added to a suspension of 4-morpholin-4-ylbenzoic acid (7.98 g, 38.5 mmol) in dry dichloromethane (DCM, 210 mL) and dimethylformamide (DMF, 0.04 mL). After refluxing the mixture for 6.5 hours, volatiles were carefully removed under reduced pressure (taking up the residue three times with toluene). The resulting 4-morpholin-4-ylbenzoyl chloride hydrochloride was added portion-wise (in about 0.5 hours) to a suspension of 5-tert-butyl 1-ethyl 3-amino-1H-thieno[2,3-c]pyrazole-1,5-dicarboxylate (6.0 g, 19.3 mmol) in dry DCM (200 mL) and pyridine (23.2 mL, 289 mmol), under stirring at 5° C. The resulting suspension was stirred for 20 hours at room temperature. 300 mL of DCM and 300 mL of aqueous sodium bicarbonate were then added to the reaction mixture; the organic layer was separated, washed with brine, dried over sodium sulphate and evaporated. Purification by chromatography (DCM/ethyl acetate 7:3) gave 4.05 g of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08481584B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-db297cc6c11440309ed910be1754bd30
출처 메모uspto-grants-2013_07