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HRID 512525作成日:2026年10月25日

Dimethylformamide → 5-(4-Acetamidobenzamido)-2-(naphthalen-1-ylamino)thiazole-4-carboxamide

https://huagongshe.com/reaction/512525

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物p-Acetamidobenzoic acidHCID 19266—
反応物Oxalyl chlorideHCID 65578—
反応物5-Amino-2-(naphthalen-1-ylamino)thiazole-4-carboxamideHCID 86703368—
溶媒PyridineHCID 1049—
溶媒TetrahydrofuranHCID 8028—
生成物5-(4-Acetamidobenzamido)-2-(naphthalen-1-ylamino)thiazole-4-carboxamideHCID 7255018929.2%

反応手順

To a mixture of 4-acetamidobenzoic acid (0.151 g, 0.845 mmol) and a catalytic amount of DMF in dry THF (8 mL) was added dropwise oxalyl chloride (0.12 mL, 1.40 mmol) at 0° C., and the mixture was stirred for 2 hrs at rt. The solvent was evaporated, and the residual oxalyl chloride was removed with azeotropic distillation using toluene under nitrogen atmosphere. The resulting acid chloride was then dissolved in pyridine (5 mL) and cooled to 0° C. To this solution, a solution of 5-amino-2-(naphthalene-1-ylamino)thiazole-4-carboxamide (0.2 g, 0.70 mmol) in pyridine (5 mL) was added at 0° C., and the mixture was stirred for 12 hrs at rt. The solvent was evaporated, and the residue was suspended into I M HCl, and the resulting solids were collected and dried. The crude solids were purified by silica gel column chromatography eluted with 3% MeOH in DCM to give 91 mg (29% yield) of the titled compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09102637B2
出典データセットuspto-grants-2015_08
ORD IDord-c9bdf21784cd4ffaae4e32a4c4f29af4
出典メモuspto-grants-2015_08