戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 962522作成日:2026年10月25日

5,10-Dihydro-11H-dibenzo(b,e)(1,4)diazepin-11-one → 10,11-Dihydro-5h-dibenzo[b,e][1,4]diazepine

https://huagongshe.com/reaction/962522

反応式

関与物質

役割名称HCID仕込み量
反応物5,10-Dihydro-11H-dibenzo(b,e)(1,4)diazepin-11-oneHCID 201327—
溶媒TetrahydrofuranHCID 8028—
生成物10,11-Dihydro-5h-dibenzo[b,e][1,4]diazepineHCID 3604679.7%

反応手順

To a stirred solution of 4.3 g of 5,11-dihydro-10H-dibenz[b,e] [1,4]diazepin-11-one in 50 ml of tetrahydrofuran, under nitrogen and cooled to 0° C. is added 4.0 ml of 10N methyl sulfide-borane complex. The ice bath is removed after 30 minutes and the reaction mixture stirred at room temperature for 18 hours. The reaction mixture is cooled in an ice bath and 30 ml of anhydrous methanol added dropwise and evaporated to dryness in vacuo. Another 30 ml of methanol is added and evaporated to a residue. The residue is quenched with 30 ml of 40% sodium hydroxide followed by heating at 110° C. for 45 minutes and cooling to room temperature. The reaction mixture is diluted with 200 ml of water and extracted with methylene chloride (3×100 ml). The combined extracts are washed with 1N HCl, water and 0.5N NaOH. The organic layer is dried and evaporated in vacuo to give 3.2 g of the desired product, m.p. 114°-116° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05760031
出典データセットuspto-grants-1998_06
ORD IDord-0794903a9f20437daf14f7ba89b061e3
出典メモuspto-grants-1998_06