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HRID 52729作成日:2026年10月26日

1-(2-isopropyloxazol-4-yl)-N-methylmethanamine → N-((N-Methyl-N-((2-isopropyl-4-oxazolyl)methyl)amino)carbonyl)-L-alanine Methyl Ester

https://huagongshe.com/reaction/52729

反応式

関与物質

役割名称HCID仕込み量
反応物1-(2-isopropyloxazol-4-yl)-N-methylmethanamineHCID 10820784—
反応物Methyl N-[(4-nitrophenoxy)carbonyl]-L-valinateHCID 15344176—
反応物N-(((4-nitrophenyl)oxy)carbonyl)-L-alanine methyl esterHCID 54298210—
生成物N-((N-Methyl-N-((2-isopropyl-4-oxazolyl)methyl)amino)carbonyl)-L-alanine Methyl EsterHCID 1070811466%

反応手順

Using the procedure of Example 1S, but replacing 2-isopropyl-4-(((N-methyl)amino)methyl)thiazole with 2-isopropyl-4-(((N-methyl)amino)methyl)-oxazole and relacing N-(((4-nitrophenyl)oxy)carbonyl)-L-valine methyl ester with N-(((4-nitrophenyl)oxy)carbonyl)-L-alanine methyl ester provided the desired compound in 66% yield. 1H NMR (CDCl3) δ1.32 (d, 6H), 1.42 (d, 3H), 2.96 (s, 3H), 3.05 (m, 1H), 3.75 (s, 3H), 4.30 (s, 2H), 4.47 (m, 1H), 5.80 (br d, 1H), 7.46 (s, 1H). Mass spectrum: (M+H)+ =284.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05616720
出典データセットuspto-grants-1997_04
ORD IDord-636ca2154b8340fd87a2cf1b2626271e
出典メモuspto-grants-1997_04