戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 563134作成日:2026年10月26日

m-(Trifluoromethyl)cinnamic acid → N-[(S)-1-benzyl-2-(4-benzyl-piperazin-1-yl)-2-oxo-ethyl]-N-(4-pentyl-benzyl)-3-(3-trifluoromethyl-phenyl)-acrylamide

https://huagongshe.com/reaction/563134

反応式

関与物質

役割名称HCID仕込み量
反応物m-(Trifluoromethyl)cinnamic acidHCID 719451—
反応物1-(4-benzyl-piperazin-1-yl)-(S)-2-(4-pentyl-benzylamino)-3-phenyl-propan-1-oneHCID 59808255—
生成物N-[(S)-1-benzyl-2-(4-benzyl-piperazin-1-yl)-2-oxo-ethyl]-N-(4-pentyl-benzyl)-3-(3-trifluoromethyl-phenyl)-acrylamideHCID 6700529969.9%

反応手順

Acylation of 1-(4-benzyl-piperazin-1-yl)-(S)-2-(4-pentyl-benzylamino)-3-phenyl-propan-1-one (43.5 mg, 0.09 mmol) according to the procedure described for the preparation of Example 1 with trans-3-trifluoromethyl-cinnamic acid (21.4 mg, 0.099 mmol) gave 42.9 mg (69%) of N—[(S)-1-benzyl-2-(4-benzyl-piperazin-1-yl)-2-oxo-ethyl]-N-(4-pentyl-benzyl)-3-(3-trifluoromethyl-phenyl)-acrylamide. LC-MS: tR=1.02 min; [M+H]+=682.48.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08067419B2
出典データセットuspto-grants-2011_11
ORD IDord-54732595803e48a389fc5d5c3246b3fc
出典メモuspto-grants-2011_11