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HRID 629706作成日:2026年10月26日

tert-butyl (2R,5S)-2-[(2-aminopyridin-3-yl)ethynyl]-5-({[tert-butyl(dimethyl)silyl]oxy}methyl)morpholine-4-carboxylate → tert-butyl (2R,5S)-2-[2-(2-aminopyridin-3-yl)ethyl]-5-({[tert-butyl(dimethyl)silyl]oxy}methyl)morpholine-4-carboxylate

https://huagongshe.com/reaction/629706

反応式

関与物質

役割名称HCID仕込み量
反応物tert-butyl (2R,5S)-2-[(2-aminopyridin-3-yl)ethynyl]-5-({[tert-butyl(dimethyl)silyl]oxy}methyl)morpholine-4-carboxylateHCID 86726311—
触媒PalladiumHCID 23938—
溶媒2,2,2-TrifluoroethanolHCID 6409—
生成物tert-butyl (2R,5S)-2-[2-(2-aminopyridin-3-yl)ethyl]-5-({[tert-butyl(dimethyl)silyl]oxy}methyl)morpholine-4-carboxylateHCID 86726313—

反応手順

To tert-butyl (2R,5S)-2-[(2-aminopyridin-3-yl)ethynyl]-5-({[tert-butyl(dimethyl)silyl]oxy}methyl)morpholine-4-carboxylate (1 eq.) in 2,2,2,-trifluoroethanol (0.4 M) at rt was added 10% Pd/C (0.2 eq.). The reaction was degassed and then shaken under 1 atm of H2 for 24 hrs. The reaction mixture was filtered on celite and concentrated to afford the desired compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09315475B2
出典データセットuspto-grants-2016_04
ORD IDord-89f2c3218b814a1681e58a1876a17109
出典メモuspto-grants-2016_04