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HRID 469324作成日:2026年10月26日

Thionyl Chloride → 6-(3,6-dichloro-pyridazine-4-carbonyl)-4-methyl-3H-benzoxazol-2-one

https://huagongshe.com/reaction/469324

反応式

関与物質

役割名称HCID仕込み量
反応物Thionyl ChlorideHCID 24386—
反応物3,6-Dichloropyridazine-4-carboxylic acidHCID 433804—
反応物Aluminum(III) ChlorideHCID 6451240—
反応物4-Methyl-3H-benzooxazol-2-oneHCID 12709336—
溶媒1,2-DichloroethaneHCID 11—
生成物6-(3,6-dichloro-pyridazine-4-carbonyl)-4-methyl-3H-benzoxazol-2-oneHCID 58181184—

反応条件

温度100 °C

反応手順

2.00 mL (27.4 mmol) thionyl chloride were added to 1.92 g (9.95 mmol) 3,6-dichloro-pyridazine-4-carboxylic acid in 10 mL 1,2-dichloroethane and the mixture was refluxed for 2 h. The reaction mixture was evaporated to dryness and coevaporated with 1,2-dichloroethane. Then 5.30 g (39.8 mmol) aluminium trichloride and 1.56 g (10.5 mmol) 4-methyl-3H-benzoxazol-2-one were added and the mixture was stirred for 1 h at 100° C. under a nitrogen atmosphere. Then it was stirred for a further 2 h at 120° C., 3 h at 130° C. and then cooled for 48 h at RT. The mixture was decomposed with ice water and extracted with DCM. The organic phases were combined, washed with water, dried on sodium sulphate, filtered and evaporated down i. vac. The residue was triturated with DIPE, suction filtered and dried.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08629137B2
出典データセットuspto-grants-2014_01
ORD IDord-cc30edbc4c1543d59c80220e9fc8cade
出典メモuspto-grants-2014_01