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HRID 512529作成日:2026年10月27日

4-Methyl-3-nitrobenzoyl chloride → 5-(4-Methyl-3-nitrobenzamido)-2-(naphthalen-2-ylamino)thiazole-4-carboxamide

https://huagongshe.com/reaction/512529

反応式

関与物質

役割名称HCID仕込み量
反応物4-Methyl-3-nitrobenzoyl chlorideHCID 66323—
反応物5-Amino-2-(naphthalen-2-ylamino)thiazole-4-carboxamideHCID 86703369—
溶媒PyridineHCID 1049—
生成物5-(4-Methyl-3-nitrobenzamido)-2-(naphthalen-2-ylamino)thiazole-4-carboxamideHCID 8670337166%

反応手順

To a mixture of 5-amino-2-(naphthalen-2-ylamino)thiazole-4-carboxamide (0.2 g, 0.70 mmol) in pyridine (5 mL) was added a solution of 4-methyl-3-nitrobenzoyl chloride in pyridine (3 mL) at 0° C. under nitrogen atmosphere. The mixture was allowed to warm up to rt, and stirred for 16 hrs at rt. The solvent was evaporated, and the crude residue was suspended into EtOAc (20 mL). The resulting solids were collected by filtration and washed with MeOH (2×5 mL) to give 0.21 g (66% 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-85ebdae6dd3244adadaa17d15c588fcb
出典メモuspto-grants-2015_08