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HRID 36118作成日:2026年10月26日

7-methyl-2-propyl-3-[2'-(aminosulfonyl)[1,1']-biphenyl-4-yl]methyl-6-[(1-oxobutyl)amino]-3H-imidazo[4,5-b]pyridine → 6-amino-7-methyl-2-propyl-3-[2'-(aminosulfonyl)[1,1']-biphenyl-4-yl]methyl-3H-imidazo[4,5-b]pyridine

https://huagongshe.com/reaction/36118

反応式

関与物質

役割名称HCID仕込み量
反応物7-methyl-2-propyl-3-[2'-(aminosulfonyl)[1,1']-biphenyl-4-yl]methyl-6-[(1-oxobutyl)amino]-3H-imidazo[4,5-b]pyridineHCID 19939752—
溶媒Hydrochloric AcidHCID 313—
溶媒MethanolHCID 887—
生成物6-amino-7-methyl-2-propyl-3-[2'-(aminosulfonyl)[1,1']-biphenyl-4-yl]methyl-3H-imidazo[4,5-b]pyridineHCID 19939763—

反応条件

温度50 °C

反応手順

A mixture of 7-methyl-2-propyl-3-[2'-(aminosulfonyl)[1,1']biphenyl-4-yl]methyl-6-[(1-oxobutyl)amino]-3H-imidazo[4,5-b]pyridine (180 mg) in 10 mL of MeOH and 1 mL of conc aqueous HCl was heated to 50° C. for 30 h. The MeOH was removed in vacuo and 100 mL of CH2Cl2 was added. The mixture was washed with saturated aqueous NaHC03 (2×30 mL), dried (Na2SO4), and concentrated to give the title compound as a foam.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05412097
出典データセットuspto-grants-1995_05
ORD IDord-e97dca0464ab4c6c8b69dcbd3d005d6c
出典メモuspto-grants-1995_05