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HRID 14848作成日:2026年10月24日

Glycine, N-[(1,1-dimethylethoxy)carbonyl]-N-methyl- → {[[3-(2-Chloro-pyrimidin-4-yl)-benzyl]-(2-hydroxy-1-methyl-ethyl)-carbamoyl]-methyl}-methyl-carbamic acid tert-butyl ester

https://huagongshe.com/ja/reaction/14848

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2-(S)-[3-(2-Chloro-pyrimidin-4-yl)-benzylamino]-propan-1-olHCID 86603286—
生成物{[[3-(2-Chloro-pyrimidin-4-yl)-benzyl]-(2-hydroxy-1-methyl-ethyl)-carbamoyl]-methyl}-methyl-carbamic acid tert-butyl esterHCID 86603287—

反応手順

Intermediate 73 was coupled with (tert-butoxycarbonyl-methyl-amino)-acetic acid following procedure K. LC-MS showed the product had the expected M+H+ of 449. 1H NMR (Varian 300 MHz, CDCl3, shifts relative to the solvent peak at 7.24 ppm) δ 8.6 (m, 1H) 8.1 (m, 1H) 8.0 (m, 1H) 7.7 (m, 1H) 7.5 (m, 2H) 4.6 (m, 2H) 4.3 (m, 2H) 4.0 (m, 1H) 3.7 (s, 1H) 3.5 (s, 1H) 3.0 (m, 4H) 1.4 (m, 9H) 1.2 (m, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732444B2
出典データセットuspto-grants-2010_06
ORD IDord-710cd64bc26e44aabf1683504209a7b2
出典メモuspto-grants-2010_06