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HRID 264695作成日:2026年10月26日

Triethylamine → (2R*,4S*)-2-benzyl-1-(3,5-dichlorobenzoyl)-N-(5-methoxy-2-indolylcarbonyl)-4-piperidinamine

https://huagongshe.com/reaction/264695

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物5-Methoxyindole-2-carboxylic acidHCID 20401—
反応物Bis(2-oxo-3-oxazolidinyl)phosphinic chlorideHCID 152842—
反応物(2R*,4S*)-2-benzyl-1-(3,5-dichlorobenzoyl)-4-piperidinamineHCID 53839030—
生成物(2R*,4S*)-2-benzyl-1-(3,5-dichlorobenzoyl)-N-(5-methoxy-2-indolylcarbonyl)-4-piperidinamineHCID 56983424—

反応手順

200 mg (0.550 mmol) of (2R*,4S*)-2-benzyl-1-(3,5-dichlorobenzoyl)-4-piperidinamine are reacted in analogy to Example 4a with 126 mg (0.661 mmol) of 5-methoxyindole-2-carboxylic acid, 168 mg (0.661 mmol) of bis(2-oxo-3-oxazolidinyl)phosphinic chloride and 169 μl (1.21 mmol) of triethylamine. The title compound ##STR88## is obtained (118 mg, 41%) as white crystals of melting point 251° C. TLC:methylene chloride/methanol/cone. ammonia (2000:50:1) Rf =0.81, FD-MS:M+ =535, 537; IR:3440, 3280, 1625 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-28513836669d468b9291b432af42b34b
出典メモuspto-grants-1997_07