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HRID 862464作成日:2026年10月25日

1-Hydroxybenzotriazole → 10,11-DIHYDRO-5-[1-(1-(4-PYRIDYL)METHYLCARBONYL)-4-PIPERIDYLIDENE]-5H-DIBENZO[a,d]CYCLOHEPTENE

https://huagongshe.com/reaction/862464

反応式

関与物質

役割名称HCID仕込み量
反応物1-HydroxybenzotriazoleHCID 75771—
反応物4-Pyridineacetic acid hydrochlorideHCID 81097—
反応物Desloratadine impurity 24HCID 1201458—
溶媒DimethylformamideHCID 6228—
生成物10,11-DIHYDRO-5-[1-(1-(4-PYRIDYL)METHYLCARBONYL)-4-PIPERIDYLIDENE]-5H-DIBENZO[a,d]CYCLOHEPTENEHCID 22621920—

反応手順

Dissolve 0.15 g (0.6m mole) of 10,11-dihydro-5-(4-piperidylidene)-5H-dibenzo[a,d]cycloheptene, 0.096 g (0.55 m mole) of 4-pyridylacetic acid hydrochloride, 0.16 g (0.83 m mole) of DEC and 0.075 g (0.55 m mole) of HOBT in 5 mL of DMF and stir at room temperature for 18 hours under nitrogen. Concentrate under vacuo and partition between 100 mL each of EtOAc and 10% aqueous sodium hydrogenphosphate. Dry the organic layer over MgSO4 and concentrate under vacuo. The resulting residue is chromatographed on silica gel using 98% dichloro methane and 2% MeOH, saturated with ammonia as the solvent, giving the product as a white waxy solid, mp=162.8°-163.4° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05719148
出典データセットuspto-grants-1998_02
ORD IDord-9d9d0685737a407fb88e879da6c516c8
出典メモuspto-grants-1998_02