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HRID 264667作成日:2026年10月25日

Triethylamine → (2R*,4S*)-2-benzyl-1-(3,5-dibromobenzoyl)-N-(4-quinolylmethyl)-N-trifluoroacetyl-4-piperidinamine

https://huagongshe.com/reaction/264667

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Benzoic acid, 3,5-dibromo-HCID 12063—
反応物Thionyl ChlorideHCID 24386—
反応物(2R*,4S*)-2-Benzyl-N-(4-quinolylmethyl)-N-trifluoroacetyl-4-piperidinamineHCID 57202094—
生成物(2R*,4S*)-2-benzyl-1-(3,5-dibromobenzoyl)-N-(4-quinolylmethyl)-N-trifluoroacetyl-4-piperidinamineHCID 5715208752.1%

反応手順

197 mg (0.70 mmol) of 3,5-dibromobenzoic acid (prepared according to J. Organometallic Chem. 215, 281 (1981)) are reacted in analogy to Example 2a first with 2 ml (27 mmol) of thionyl chloride and subsequently with 200 mg (0.468 mmol) of (2R*,4S*)-2-benzyl-N-(4-quinolylmethyl)-N-trifluoroacetyl-4-piperidinamine and 130 μl (0.936 mmol) of triethylamine to give the title compound (168 mg, 52%). TLC: methylene chloride/methanol/conc. ammonia (700:50:1) Rf =0.60, FD-MS: M+ =687, 689, 691.

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-58665b85ed9a4b18833bf340f9db69b6
出典メモuspto-grants-1997_07