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HRID 1156365作成日:2026年10月27日

Methanol → 3-(2-(4-((4-Fluorophenyl)hydroxymethyl)-1-piperidinyl)ethyl)-2,4(1H,3H)-quinazolinedione

https://huagongshe.com/reaction/1156365

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物KetanserinHCID 3822—
反応物Sodium borohydrideHCID 4311764—
溶媒WaterHCID 962—
生成物3-(2-(4-((4-Fluorophenyl)hydroxymethyl)-1-piperidinyl)ethyl)-2,4(1H,3H)-quinazolinedioneHCID 156394—

反応手順

To a stirred mixture of 2.6 parts of 3-[2-[4-(4-fluorobenzoyl)-1-piperidinyl]ethyl]-2,4-(1H,3H)-quinazolinedione and 120 parts of methanol are added portionwise 2 parts of sodium borohydride. Upon completion, stirring is continued overnight at room temperature. Water is added and the whole is evaporated. The residue is stirred in water. The solid product is filtered off and crystallized from 2-propanone, yielding 1.2 parts of 3-[2-[4-[(4-fluorophenyl)hydroxymethyl]-1-piperidinyl]ethyl]-2,4(1H,3H)-quinazolinedione; mp. 212.8° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04335127
出典データセットuspto-grants-1982_06
ORD IDord-45be1c0b95f7485189ed572b20128d75
出典メモuspto-grants-1982_06