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HRID 275620作成日:2026年10月27日

N-Boc-beta-(2-thienyl)-DL-alanine → (RS)-alpha-amino-N-[(1S,2R,3S)-1-(cyclohexylmethyl)-3-cyclopropyl-2,3-dihydroxypropyl]-3-(thiophen-2-yl)propionamide

https://huagongshe.com/reaction/275620

反応式

関与物質

役割名称HCID仕込み量
反応物N-Boc-beta-(2-thienyl)-DL-alanineHCID 5035100—
反応物(1S,2R,3S)-3-amino-4-cyclohexyl-1-cyclopropyl-1,2-butanediolHCID 14930738—
生成物(RS)-alpha-amino-N-[(1S,2R,3S)-1-(cyclohexylmethyl)-3-cyclopropyl-2,3-dihydroxypropyl]-3-(thiophen-2-yl)propionamideHCID 57152908—

反応手順

In an analogous manner to that described above, by the condensation of rac-α-(tert-butoxyformamido)-3-(thiophen-2-yl)propionic acid [Pol. J. Chem. 54(11-12), 2225 (1980)] and (1S,2R,3S)-3-amino-4-cyclohexyl-1-cyclopropyl-1,2-butanediol followed by acidic hydrolysis there was obtained (RS)-α-amino-N-[(1S,2R,3S)-1-(cyclohexylmethyl)-3-cyclopropyl-2,3-dihydroxypropyl]-3-(thiophen-2-yl)propionamide, MS: 381 (M+H)+ as a colourless foam.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05393875
出典データセットuspto-grants-1995_02
ORD IDord-3440aedb76e14389b64ed709460c5ea7
出典メモuspto-grants-1995_02