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HRID 218481作成日:2026年10月24日

Sodium Bicarbonate → 1,4-dihydro-4-(1H-indazol-5-yl)-2,6-dimethyl-3,5-pyridinedicarbonitrile

https://huagongshe.com/ja/reaction/218481

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium BicarbonateHCID 516892—
反応物(2Z)-3-Amino-2-butenenitrileHCID 5325263—
反応物1H-Indazole-5-carboxaldehydeHCID 21250644—
溶媒Acetic AcidHCID 176—
生成物1,4-dihydro-4-(1H-indazol-5-yl)-2,6-dimethyl-3,5-pyridinedicarbonitrileHCID 2495910444%

反応手順

A mixture of 1H-indazole-5-carboxaldehyde from Synthetic Preparation 1 (447 mg, 3.1 mmol) and 3-aminocrotononitrile (526.4 mg, 6.41 mmol) in HOAc (10 mL) was kept at 110° C. for 1.5 hr, after which it was cooled to rt. The reaction was treated with NaHCO3 (sat.) to pH 10, and extracted with EtOAc. The organic phases were combined, washed with brine, and dried. Concentration followed by purification with flash chromatography afforded 1,4-dihydro-4-(1H-indazol-5-yl)-2,6-dimethyl-3,5-pyridinedicarbonitrile (370 mg, 44%) (Cpd. No. 80, Table 2). 1H-NMR (400 MHz, CDCl3): δ=8.07 (s, 1H), 7.64 (s, 1H), 7.53 (d, 1H), 7.35 (d, 1H), 4.48 (s, 1H), 2.03 (s, 6H) ppm.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08198456B2
出典データセットuspto-grants-2012_06
ORD IDord-279b7ddbe4b742d7b415f99edaec384d
出典メモuspto-grants-2012_06