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HRID 416851作成日:2026年10月27日

Sodium Dithionite → HCID 178488872、化合物

https://huagongshe.com/reaction/416851

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium DithioniteHCID 24489—
反応物4-MethoxybenzaldehydeHCID 31244—
反応物5-Bromo-4-(4-((6-methoxypyridin-3-yl)methyl)piperazin-1-yl)-3-nitropyridin-2-amineHCID 57897154—
反応物HCID 178482685HCID 178482685—
溶媒EthanolHCID 702—
溶媒DimethylformamideHCID 6228—
生成物HCID 178488872HCID 17848887256%

反応手順

This was prepared using the same procedure as for 4-(6-bromo-2-(4-(dimethylamino)phenyl)-3H-imidazo[4,5-b]pyridin-7-yl)-N-phenylpiperazine-1-carboxamide, but here using 5-bromo-4-(4-((6-methoxypyridin-3-yl)methyl)piperazin-1-yl)-3-nitropyridin-2-amine (30 mg, 0.071 mmol), DMF (0.15 mL), ethanol (0.85 mL), 1M Na2S2O4 (3 eq, 0.21 mmol, 0.21 mL) and 4-methoxybenzene carboxaldehyde (1.1 eq, 0.078 mmol, 10 mg). After 6 h, concentration in vacuo and purification by preparative tlc (CH2Cl2-MeOH, 95:5) gave the product (20 mg, 56%) as a colourless solid; δH (500 MHz, DMSO-d6) 2.60 (s, br, 4H, piperazine N(CH2)2), 3.52 (s, 2H, NCH2), 3.64 (t, J=4.5 Hz, 4H, piperazine N(CH2)2), 3.84 (s, 3H, OCH3), 3.85 (s, 3H, OCH3), 6.81 (d, J=8.5 Hz, 1H, methoxypyridine H-5), 7.09 (d, J=8.9 Hz, 2H, methoxyphenyl H-2 & H-6), 7.70 (dd, J=8.5, 2.6 Hz, 1H, methoxypyridine H-4), 8.11 (d, J=2.3 Hz, 1H, methoxypyridine H-2), 8.20 (s, 1H, imidazo[4,5-b]pyridine H-5), 13.34 (s, br, 1H, imidazo[4,5-b]pyridine NH);

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08088761B2
出典データセットuspto-grants-2012_01
ORD IDord-46fb68b42cca485c956f9154defe97ad
出典メモuspto-grants-2012_01