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HRID 253689作成日:2026年10月26日

Sodium Iodide → HCID 66866083、化合物

https://huagongshe.com/reaction/253689

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium IodideHCID 5238—
反応物TriethylamineHCID 8471—
反応物6-(4-Bromobutyloxy)indanoneHCID 11550940—
反応物1-(2,3-Dichlorophenyl)piperazine hydrochlorideHCID 11630372—
溶媒ChloroformHCID 6212—
溶媒AcetonitrileHCID 6342—
生成物HCID 66866083HCID 66866083—

反応手順

A mixture of 6-(4-bromobutoxy)-indan-1-one prepared by the process described in step (1) above (100 gm, 0.282 mol, 80% purity) and sodium iodide (42 gm, 0.28 mol) in acetonitrile was refluxed for 30 minutes and then cooled to room temperature. 1-(2,3-dichlorophenyl)-piperazine hydrochloride (68 gm, 0.294 mol) and triethyl amine (77 gm, 0.761 mol) were added to the mixture and the resulting mixture was refluxed for 4-6 hr. After solvent was removed, the residue thus obtained was dissolved in chloroform, washed with water which treatment with chloroform and Hydrochloric acid gave 140 g of 6-[4-[4-(2,3-dichlorophenyl)-1-piperazinyl]butoxy]-indan-1-one hydrochloride. This on chloroform solution was basified with ammonium hydroxide to pH 9.5 and extracted with chloroform twice 2×500 ml. The combined chloroform layer was concentrated using rotavapour under reduced pressure to get a residue which on purification with methanol gave 85 gm of 6-[4-[4-(2,3-dichlorophenyl)-1-piperazinyl]-butoxy]-indan-1-one of the formula 2 which has identical characteristic of product obtained for the Example 1, step-2.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07872132B2
出典データセットuspto-grants-2011_01
ORD IDord-a1de4719d7404802b28903a7d008e2d9
出典メモuspto-grants-2011_01