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HRID 486663作成日:2026年10月26日

Trimethyl orthobeznoate → 4,5-dihydro-3-methyl-4-(3-methyl-2-thienyl)-2-phenyl-3H-1,3-benzodiazepine

https://huagongshe.com/reaction/486663

反応式

関与物質

役割名称HCID仕込み量
反応物Trimethyl orthobeznoateHCID 69720—
反応物Compound 7189HCID 130176—
溶媒Acetic AcidHCID 176—
生成物4,5-dihydro-3-methyl-4-(3-methyl-2-thienyl)-2-phenyl-3H-1,3-benzodiazepineHCID 2241448491.4%

反応手順

A stirred solution of 2.19 g of 2-amino-N-methyl-α-(3-methyl-2-thienyl)benzeneethanamine and 9.88 g of trimethyl orthobenzoate was treated rapidly with 2.4 ml of glacial acetic acid, and heated under reflux for 8 hours. The solution was concentrated at 75° C. on a rotary evaporator (vacuum pump) to a syrup. The syrup was then partioned between 10% hydrochloric acid solution (50 ml) and ether. The aqueous phase was extracted again with ether, basified with 10% sodium hydroxide solution (60 ml) and extracted with dichloromethane (2×100 ml). The combined organic phase was dried over anhydrous sodium sulfate, filtered, and concentrated to an oil. The oil was purified by preparative HPLC (Water's Associates Prep LC/System 500A, silica gel, sample applied in dichloromethane, 2% triethylamine in methanol as the eluent). Concentration of the appropriate fractions yielded 2.70 g of 4,5-dihydro-3-methyl-4-(3-methyl-2-thienyl)-2-phenyl-3H-1,3-benzodiazepine as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05292760
出典データセットuspto-grants-1994_03
ORD IDord-b2402df29d2f4739ade6369bee54556e
出典メモuspto-grants-1994_03