Benzene → Ethyl 1-(1-methylethyl)-6-phenyl-1H-pyrazolo[3,4-b]pyridine-4-carboxylate

関与物質

役割	名称	HCID	仕込み量
反応物	Benzene	HCID 241	—
反応物	2,4-Dioxo-4-phenyl-butyric acid ethyl ester	HCID 226503	—
反応物	1-(propan-2-yl)-1H-pyrazol-5-amine	HCID 1090341	—
溶媒	Acetic Acid	HCID 176	—
生成物	Ethyl 1-(1-methylethyl)-6-phenyl-1H-pyrazolo[3,4-b]pyridine-4-carboxylate	HCID 46538388	—

反応手順

The title compound was prepared in the same manner as described for intermediate 61 using ethyl 2,4-dioxo-4-phenylbutanoate (5 g, 22.7 mmol), 1-(1-methylethyl)-1H-pyrazol-5-amine (2.84 g, 22.7 mmol), benzene (70 mL), and acetic Acid (44 mL) The crude product was purified by silica gel chromatography (eluent: 0 to 100% EtOAc/hexanes) to give 6.72 g (95%) as a pale yellow solid. LCMS E-S (M+H)=310.5. 1H NMR (400 MHz, DMSO-d6) δ 8.39 (s, 1H), 8.17-8.28 (m, 3H), 7.49-7.64 (m, 3H), 5.38 (quin, J=6.69 Hz, 1H), 4.49 (q, J=7.07 Hz, 2H), 1.57 (d, J=6.57 Hz, 6H), 1.44 (t, 3H).

情報源と証拠

DOI	10.6084/m9.figshare.5104873.v1
特許番号	US08637509B2
出典データセット	uspto-grants-2014_01
ORD ID	ord-de00594635b0481c88e99866406d9e72
出典メモ	uspto-grants-2014_01