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HRID 2427957作成日:2026年10月25日

Ammonia → 2-(3-Hydroxyphenyl)-9-(2-methoxyphenyl)-9H-purine-6-carboxamide

https://huagongshe.com/reaction/2427957

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物Ethyl 5-amino-2-(3-hydroxyphenyl)-6-(2-methoxyphenylamino)pyrimidine-4-carboxylateHCID 57474574—
反応物5-Amino-2-(3-hydroxyphenyl)-6-(2-methoxyphenylamino)pyrimidine-4-carboxamideHCID 57474576—
溶媒MethanolHCID 887—
生成物2-(3-Hydroxyphenyl)-9-(2-methoxyphenyl)-9H-purine-6-carboxamideHCID 5747456899%

反応手順

5-Amino-2-(3-hydroxyphenyl)-6-(2-methoxyphenylamino)pyrimidine-4-carboxamide. A solution of ethyl 5-amino-2-(3-hydroxyphenyl)-6-(2-methoxyphenylamino)pyrimidine-4-carboxylate. (57.8 mg, 0.152 mmol) in anhydrous methanol (5 mL) was chilled to −78° C. The solution was then saturated with ammonia gas. The reaction vessel was sealed at −78° C. and allowed to warm to room temperature. After 18 h the reaction was chilled to −78° C. and opened to atmosphere. The volatiles were evaporated and the resulting material was purified by column chromatography (SiO2, 2% to 5% methanol in methylene chloride) to provide the title compound in 98.3% purity (53 mg, 0.151 mmol, 99% yield). 1H NMR (400 MHz, CD3OD) δ 8.41 (m, 1H), 7.79 (dt, J=8.00, 1.20, 1H), 7.73 (m, 1H), 7.21 (t, J=8.00, 1H), 7.06 (m, 3H), 6.79 (ddd, J=8.00, 2.54, 0.98, 1H), 3.94 (s, 3H); MS (ESI) m/z 352.2 [M+1]+; mp: 230-231° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07968556B2
出典データセットuspto-grants-2011_06
ORD IDord-3175ac30b42a4d7fb0ee011b22e20798
出典メモuspto-grants-2011_06