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HRID 590524作成日:2026年10月27日

Ammonia → HCID 118033080、化合物

https://huagongshe.com/reaction/590524

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物Ammonium iodideHCID 25487—
反応物1'-Methyl-2'-(methylthio)-6,7-dihydro-5H-spiro[benzo[b]thiophene-4,4'-imidazol]-5'(1'H)-oneHCID 118033078—
溶媒MethanolHCID 887—
生成物HCID 118033080HCID 118033080—

反応手順

1′-Methyl-2′-(methylthio)-6,7-dihydro-5H-spiro[benzo[b]thiophene-4,4′-imidazol]-5′(1′H)-one (1.5 g, 5.63 mmol), ammonium iodide (4.89 g, 33.78 mmol) and 7 N ammonia in methanol (20 mL) were heated at 90° C. for 12 h. The solvent was then evaporated under reduced pressure and the residue was partitioned between water and dichloromethane. The dichloromethane extracts were combined, dried over magnesium sulphate and evaporated under reduced pressure to give an oil. This consisted of the title compound as the major component and its minor regioisomer in a 2:1 ratio. The oil was loaded onto a Biotage SNAP cartridge and eluted with dichloromethane-dichloromethane/7N ammonia in methanol (9:1). The appropriate fractions were combined and evaporated under reduced pressure to give 2′-amino-1′-methyl-6,7-dihydro-5H-spiro[benzo[b]thiophene-4,4′-imidazol]-5′(1′H)-one as a foam (800 mg, 60%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09233982B2
出典データセットuspto-grants-2016_01
ORD IDord-8272d6434bfd4a528cc703711973edfa
出典メモuspto-grants-2016_01