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HRID 9287作成日:2026年10月25日

Hydrazine → HCID 178418907、化合物

https://huagongshe.com/reaction/9287

反応式

関与物質

役割名称HCID仕込み量
反応物HydrazineHCID 9321—
反応物Potassium HydroxideHCID 14797—
反応物HCID 178418911HCID 178418911—
溶媒WaterHCID 962—
溶媒Diethylene GlycolHCID 8117—
溶媒Sodium BicarbonateHCID 516892—
生成物HCID 178418907HCID 178418907—

反応条件

温度170 °C

反応手順

Use of 7,8-dihydro-6H-quinolin-5-one (Intermediate TWENTYTWO-1) (obtained as described in Molina, et. al. Tetrahedron 1995, 51, 1265, incorporated herein by reference) in Method E produced 6-(1H-imidazol-4-ylmethyl)-7,8-dihydro-6H-quinolin-5-one (Intermediate TWENTYTWO-2). To a solution of 6-(1H-imidazol-4-ylmethyl)-7,8-dihydro-6H-quinolin-5-one (Intermediate TWENTYTWO-2) (1.31 g, 227 mmol) in diethylene glycol (10 mL) was added hydrazine (6.3 mL, 200 mmol) followed by KOH (4.85 g, 56.2 mmol). The mixture was heated to 170° C. for 5 h. The mixture was diluted with water (200 mL) and sat. NaHCO3. The aqueous solution was extracted with CHCl3 (3×50 mL). The combined organic portions were washed with water and brine. The organic layer was dried over MgSO4, filtered and evaporated to give 6-(1H-imidazol-4-ylmethyl)-5,6,7,8-tetrahydro-quinoline as a foamy solid, 1.15 g (92%). By the applicable process steps described in Method A, the imidazole compound was used to produce 4-(5,6,7,8-tetrahydro-quinolin-6-ylmethyl)-1,3-dihydro-imidazole-2-thione (Compound 162).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091232B2
出典データセットuspto-grants-2006_08
ORD IDord-9b9de1057bbe403baed0bb47fffa7c28
出典メモuspto-grants-2006_08