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HRID 382407作成日:2026年10月26日

Glycine, N-[(1,1-dimethylethoxy)carbonyl]-N-methyl- → 1-(4-t-butylbenzyl)-4-(2-(N-t-butyloxycarbonyl-N-methylamino)acetylamino)-5-imidazolecarboxamide

https://huagongshe.com/reaction/382407

反応式

関与物質

役割名称HCID仕込み量
反応物Glycine, N-[(1,1-dimethylethoxy)carbonyl]-N-methyl-HCID 83692—
反応物4-Amino-1-(4-t-butylbenzyl)-5-imidazolecarboxamideHCID 18360289—
生成物1-(4-t-butylbenzyl)-4-(2-(N-t-butyloxycarbonyl-N-methylamino)acetylamino)-5-imidazolecarboxamideHCID 1836041080%

反応手順

An amidation reaction and post-treatment were carried out under the same conditions as in Example 17, using 2.50 g (9.18 mmol) of 4-amino-1-(4-t-butylbenzyl)-5-imidazole carboxamide which was prepared in the same manner as in Example 57 and 2-(N-t-butyloxycarbonyl-N-methylamino)acetic acid instead of 3-pyridylacetic acid hydrochloride to obtain 3.27 g of 1-(4-t-butylbenzyl)-4-(2-(N-t-butyloxycarbonyl-N-methylamino)acetylamino)-5-imidazolecarboxamide (yield 80%).

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-d67e24fc3b63487db53ad198a385b8a3
出典メモuspto-grants-2001_10