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HRID 448129作成日:2026年10月24日

Pyridine → HCID 66784763、化合物

https://huagongshe.com/ja/reaction/448129

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物Oxalyl chlorideHCID 65578—
反応物4-(Morpholin-4-yl)benzoic acidHCID 345278—
反応物Sodium BicarbonateHCID 516892—
反応物5-tert-butyl 1-ethyl 3-amino-1H-thieno[2,3-c]pyrazole-1,5-dicarboxylateHCID 57737272—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物HCID 66784763HCID 6678476341.9%

反応条件

温度5 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08481584B2
出典データセットuspto-grants-2013_07
ORD IDord-db297cc6c11440309ed910be1754bd30
出典メモuspto-grants-2013_07