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HRID 235457作成日:2026年10月26日

Decanoyl chloride → Decanoic acid 1,1-diethyl-3-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propyl ester hydrochloride

https://huagongshe.com/reaction/235457

反応式

関与物質

役割名称HCID仕込み量
反応物Decanoyl chlorideHCID 66982—
反応物Sodium BicarbonateHCID 516892—
反応物6-Fluoro-3-[1-(3-hydroxy-3-ethylpentyl)4-piperidinyl]-1,2-benzisoxazoleHCID 18467342—
溶媒DichloromethaneHCID 6344—
生成物Decanoic acid 1,1-diethyl-3-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propyl ester hydrochlorideHCID 8674976081%

反応手順

To a solution of 6-fluoro-3-[l-(3-hydroxy-3-ethylpentyl)-4-piperidinyl]-1,2-benzisoxazole (2.5 g, 7.48 mmol) in DCM (100 ml) was added decanoyl chloride (1.5 ml, 7.48 mmol) at 0 C, under nitrogen. The reaction mixture was stirred for 4 days at which time it was poured into NaHCO3 (sat., 50 ml). The layers were separated and the aqueous phase was extracted with DCM (2X). The combined organics were dried, filtered and concentrated to give the crude product which was purified via flash column chromatography (silica gel, 20-40% EtOAc/DCM). The product containing fractions were concentrated to give 3.0 g (81%) of the desired product as a yellow oil. The hydrochloride salt was prepared in anhydrous ether (60 ml) and isopropanol (1 ml) with ethereal HCl. The white salt was filtered and washed with anhydrous ether, m.p.=159°-161° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05597842
出典データセットuspto-grants-1997_01
ORD IDord-4296c2d7ec714dbd88fa98258f5c4ed5
出典メモuspto-grants-1997_01