戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 256666作成日:2026年10月26日

Thiophene → HCID 178480440、化合物

https://huagongshe.com/reaction/256666

反応式

関与物質

役割名称HCID仕込み量
反応物ThiopheneHCID 8030—
反応物Potassium AcetateHCID 517044—
反応物HCID 178418361HCID 178418361—
反応物HCID 178419280HCID 178419280—
反応物HCID 178486302HCID 178486302—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
生成物HCID 178480440HCID 17848044056%

反応手順

A mixture of 3 parts of poly(oxymethylene), 5 parts of 7-[(4-fluorophenyl)methyl]-8-(4-piperidinylamino)-7H-purin-6-ol dihydrobromide, 1 part of a solution of thiophene in methanol 4%, 5 parts of potassium acetate and 120 parts of methanol was hydrogenated at normal pressure and at room temperature with 2 parts of palladium-on-charcoal catalyst 10%. After the calculated amount of hydrogen was taken up, the catalyst was filtered off and the filtrate was evaporated. The residue was taken up in water and the whole was treated with sodium carbonate. The product was extracted with dichloromethane. The extract was dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol, saturated with ammonia, (95:5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from acetonitrile. The product was filtered off and dried, yielding 2 parts (56%) of 7-[(4-fluorophenyl)methyl]-8-[(1-methyl-4-piperidinyl)amino] -7H-purin-6-ol; mp. 255.6° C. (compound 139).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05258380
出典データセットuspto-grants-1993_11
ORD IDord-c54705a1b31a42c2816ada1141e4e2fc
出典メモuspto-grants-1993_11