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HRID 1072000作成日:2026年10月27日

Pyridine → HCID 178440950、化合物

https://huagongshe.com/reaction/1072000

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物DimethylformamideHCID 6228—
反応物4-tert-Butylbenzyl alcoholHCID 13416—
反応物DiisopropylethylamineHCID 81531—
反応物4-Nitrophenyl chloroformateHCID 82129—
溶媒MethanolHCID 887—
溶媒DichloromethaneHCID 6344—
生成物HCID 178440950HCID 178440950—

反応手順

To a solution of 4-tert-butylbenzyl alcohol (1.97 g, 12 mmol) in DCM (30 mL) was added pyridine (1.3 mL) and then a solution of 4-nitrophenyl chloroformate (1.57 g, 7.8 mmol) in DCM (20 mL). The mixture was stirred at room temperature for 1 h, concentrated under reduced pressure, and to the residue was added a mixture of of 4,5,6,7-tetrahydromidazo[4,5-c]pyridine (1.5 g, 7 mmol), methanol (3.3 mL), DMF (30 mL), and diisopropylethylamine (4.1 mL). The resulting mixture was stirred at room temperature overnight and concentrated under reduced pressure. The residue was distributed between water and ethyl acetate, phases were separated, and the organic layer was washed with water, dried (MgSO4), and filtered. A solution of oxalic acid (0.63 g) in ethyl acetate was added to the filtrate and the mixture was allowed to stand for 24 h. Filtration yielded the title compound as colorless solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06908926B1
出典データセットuspto-grants-2005_06
ORD IDord-597b2f8d88f84ce8a7442fc7e07d1de4
出典メモuspto-grants-2005_06