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HRID 469311作成日:2026年10月27日

Dimethylformamide → 6-(2-bromo-pyridine-4-carbonyl)-4-methyl-3H-benzoxazol-2-one

https://huagongshe.com/reaction/469311

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Thionyl ChlorideHCID 24386—
反応物BromineHCID 24408—
反応物ChlorineHCID 24526—
反応物2-Bromoisonicotinic acidHCID 222701—
反応物Aluminum(III) ChlorideHCID 6451240—
反応物4-Methyl-3H-benzooxazol-2-oneHCID 12709336—
溶媒DichloromethaneHCID 6344—
生成物6-(2-bromo-pyridine-4-carbonyl)-4-methyl-3H-benzoxazol-2-oneHCID 58181213—

反応条件

温度130 °C

反応手順

2.20 mL (30.0 mmol) thionyl chloride and 0.390 mL (4.80 mmol) DMF were added to 2.00 g (9.90 mmol) 2-bromopyridine-4-carboxylic acid in 30 mL DCM and refluxed for 2 h. The reaction mixture was evaporated to dryness and coevaporated twice with toluene. The residue was combined with 6.24 g (46.8 mmol) aluminium trichloride and 1.50 g (10.1 mmol) 4-methyl-3H-benzoxazol-2-one and the mixture obtained was stirred overnight at 110° C. and for 5 hours at 130° C. The mixture was decomposed with ice water and extracted twice with DCM. The organic phases were dried on magnesium sulphate, filtered and evaporated down i. vac. The residue was triturated with DIPE/MeOH and suction filtered. The product obtained is a mixture of the corresponding bromine and chlorine compound (40/60).

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-a7869bb0c12f4d85aef225774e98f332
出典メモuspto-grants-2014_01