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HRID 2427956作成日:2026年10月25日

Potassium Phosphate, Tribasic → 2-(3-Hydroxyphenyl)-9-(2-methoxyphenyl)-9H-purine-6-carboxamide

https://huagongshe.com/reaction/2427956

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium Phosphate, TribasicHCID 62657—
反応物(3-hydroxyphenyl)boronic AcidHCID 2734359—
反応物2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
反応物Ethyl 5-amino-2-(3-hydroxyphenyl)-6-(2-methoxyphenylamino)pyrimidine-4-carboxylateHCID 57474574—
反応物Ethyl 5-amino-2-chloro-6-(2-methoxyphenylamino)pyrimidine-4-carboxylateHCID 57474575—
触媒palladium(II) acetateHCID 167845—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物2-(3-Hydroxyphenyl)-9-(2-methoxyphenyl)-9H-purine-6-carboxamideHCID 5747456812%

反応手順

Ethyl 5-amino-2-(3-hydroxyphenyl)-6-(2-methoxyphenylamino)pyrimidine-4-carboxylate. In a microwave flask was placed ethyl 5-amino-2-chloro-6-(2-methoxyphenylamino)pyrimidine-4-carboxylate (404 mg, 1.252 mmol), 3-hydroxyphenylboronic acid (259 mg, 1.878 mmol), potassium phosphate (531 mg, 2.504 mmol), dicyclohexyl(2′,6′-dimethoxybiphenyl-2-yl)phosphine (77 mg, 0.188 mmol) and palladium (II) acetate (42.2 mg, 0.188 mmol) in tetrahydrofuran (20 mL) and water (2 mL) and the reaction mixture was heated at 120° C. for 20 min in the microwave. The reaction mixture was filtered and the solvent was removed under reduced pressure. The crude material was purified by column chromatography (SiO2, 80-60% n-hexanes in ethyl acetate) and semi prep HPLC (20-100% acetonitrile+0.1% TFA in H2O+0.1% TFA, over 30 min). Fractions containing product were neutralized with potassium carbonate (saturated aqueous solution), extracted with ethyl acetate and dried over magnesium sulfate to provide the title compound (57.8 mg, 0.152 mmol, 12% yield). MS (ESI) m/z 381.4 [M+1]+.

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-7ea2bf5b7628417ea8649938874b95e4
出典メモuspto-grants-2011_06