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HRID 382397作成日:2026年10月26日

3-Pyridineacetic acid, hydrochloride (1:1) → 1-benzyl-4-(3-(N-t-butyloxycarbonyl-N-methylamino)benzoylamino)-5-imidazole carboxamide

https://huagongshe.com/reaction/382397

反応式

関与物質

役割名称HCID仕込み量
反応物3-Pyridineacetic acid, hydrochloride (1:1)HCID 2723724—
反応物1-benzyl-4-amino-1H-imidazole-5-carboxamideHCID 14000620—
反応物3-(N-Boc-N-methylamino)benzoic acidHCID 22349165—
生成物1-benzyl-4-(3-(N-t-butyloxycarbonyl-N-methylamino)benzoylamino)-5-imidazole carboxamideHCID 1836049581%

反応手順

An amidation reaction and post-treatment were carried out under the same conditions as in Example 17, using 0.65 g (3.0 mmol) of 4-amino-1-benzyl-5-imidazolecarboxamide which was prepared in the same manner as in Reference Example 2 and 3-(N-t-butyloxycarbonyl-N-methylamino)benzoic acid, instead of 3-pyridylacetic acid hydrochloride, to obtain 1.09 g of 1-benzyl-4-(3-(N-t-butyloxycarbonyl-N-methylamino)benzoylamino)-5-imidazole carboxamide (yield 81%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06310070B1
出典データセットuspto-grants-2001_10
ORD IDord-e276764799474190a0415b2940ed430a
出典メモuspto-grants-2001_10