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HRID 260339作成日:2026年10月24日

Triethylamine → 4-(4-Phenyl-butyl-carbamoyloxy)-piperidine-1-carboxylic acid 6-[(4-phenoxy-phenyl)-oxycarbonylamino]-hexyl ester

https://huagongshe.com/ja/reaction/260339

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物BenzenebutanamineHCID 83242—
反応物HCID 15293307HCID 15293307—
溶媒DichloromethaneHCID 6344—
生成物4-(4-Phenyl-butyl-carbamoyloxy)-piperidine-1-carboxylic acid 6-[(4-phenoxy-phenyl)-oxycarbonylamino]-hexyl esterHCID 983071099.3%

反応手順

A solution of 4-phenylbutylamine (610 μl, 3.86 mmol) and triethylamine (2.24 mL, 16.1 mmol) in 30 mL of methylene chloride was added under nitrogen dropwise to a solution of the carbonate prepared in Example 5 (2.0 g, 3.22 mmol) in 30 mL of methylene chloride at ice bath temperature. After the addition the cooling bath was removed and the reaction stirred at room temperature overnight. An additional 204 μl (1.29 mmol) of 4-phenylbutylamine and 180 μl (1.29 mmol) of triethylamine were added and the reaction stirred at room temperature for approximately 7 hours. The reaction was extracted one time with 1N HCl, multiple times with saturated Na2CO3, dried (MgSO4) and the solvent removed under reduced pressure to give 2.02 g of a crystalline solid. Purification of the solid on silica gel (230-400 mesh) using 5%-20% ethyl acetate-methylene chloride as the eluent gave 1.43 g (70%) of the title compounds as a white crystalline solid, mp 84°-86° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05527804
出典データセットuspto-grants-1996_06
ORD IDord-7c5876b7c39e4ce98d87d26b58205a66
出典メモuspto-grants-1996_06