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HRID 410094作成日:2026年10月24日

Diisopropylcarbodiimide → 2-{2,6-dichloro-3-[(2,2-dimethyl-propionylamino)-methyl]-phenylamino}-6-(2,2-difluoro-ethoxy)-1H-benzimidazole-5-carboxylic acid

https://huagongshe.com/ja/reaction/410094

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylcarbodiimideHCID 12734—
反応物Bis(trimethylsilyl)trifluoroacetamideHCID 94358—
反応物N-[(2,4-dichloro-3-isothiocyanatophenyl)methyl]-2,2-dimethylpropanamideHCID 56840192—
反応物2-(2,2-Difluoro-ethoxy)-4,5-diamino-benzoic acidHCID 87139723—
溶媒Acetic AcidHCID 176—
溶媒AcetonitrileHCID 6342—
生成物2-{2,6-dichloro-3-[(2,2-dimethyl-propionylamino)-methyl]-phenylamino}-6-(2,2-difluoro-ethoxy)-1H-benzimidazole-5-carboxylic acidHCID 178447326—

反応手順

A mixture of 2-(2,2-difluoro-ethoxy)-4,5-diamino-benzoic acid (732 mg, 3.15 mmol), N-(2,4-dichloro-3-isothiocyanato-benzyl)-2,2-dimethyl-propionamide (1.00 g, 3.15 mmol) and MeCN (15 mL) is stirred for 48 h, then BSTFA (1.03 mL, 3.15 mmol) is added and it is stirred at reflux for 10 min. Then DIC (0.494 mL, 3.15 mmol) is added and it is stirred for another 4 h. The mixture is cooled to rt, diluted with HOAc and concentrated. The residue is stirred with 1N NaOH, filtered and the filtrate is acidified with 4N HCl, extracted with EtOAc and purified via chromatography [DCM→DCM+10% EtOH/HOAc (95:5)] to give the subtitle compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08759537B2
出典データセットuspto-grants-2014_06
ORD IDord-0b47fcdd7a18489ca43242e7456eac42
出典メモuspto-grants-2014_06