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HRID 264703作成日:2026年10月27日

Acetic Acid → (2R*,4S*)-2-benzyl-1-(3,5-dichlorobenzoyl)-N-diphenylmethyl-4-piperidinamine

https://huagongshe.com/reaction/264703

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物BenzophenoneHCID 3102—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物2-Benzyl-1-(3,5-dichlorobenzoyl)-4-piperidinamineHCID 21220201—
溶媒TolueneHCID 1140—
生成物(2R*,4S*)-2-benzyl-1-(3,5-dichlorobenzoyl)-N-diphenylmethyl-4-piperidinamineHCID 57170253—

反応手順

A solution of 200 mg (0.551 mmol) of (2R*,45*)-2-benzyl-1-(3,5-dichlorobenzoyl)-4-piperidinamine and 110 mg (0.606 mmol) of benzophenone in 5 ml of toluene are kept at reflux for 18 hours. The reaction mixture is then concentrated in a rotary evaporator and dissolved in 3 ml of methanol, and 69 mg (1.10 mmol) of sodium cyanoborohydride are added at RT. The reaction mixture is adjusted to pH=5 with 80 μl of acetic acid and stirred at RT for 68 hours. The title compound ##STR98## is obtained as white foam (120 mg, 41%). TLC:toluene/ethyl acetate (7:3) Rf =0.79, FD-MS:M+ =528, 530; IR:1630 cm-1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05646144
出典データセットuspto-grants-1997_07
ORD IDord-ffd66f18dc844192b04fcf55fc735a75
出典メモuspto-grants-1997_07