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HRID 25165作成日:2026年10月26日

Dimethylformamide → N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-6-cyanopyrrolo[1,2-a]pyrazine-3-carboxamide Tartrate

https://huagongshe.com/reaction/25165

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物D-Tartaric acidHCID 439655—
反応物N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-6-bromopyrrolo[1,2-a]pyrazine-3-carboxamideHCID 10247203—
触媒Zinc cyanide (Zn(CN)2)HCID 11186—
触媒HCID 178418397HCID 178418397—
生成物N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-6-cyanopyrrolo[1,2-a]pyrazine-3-carboxamide TartrateHCID 6977193347%

反応条件

温度95 °C

反応手順

To an argon sparged solution of N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-6-bromopyrrolo[1,2-a]pyrazine-3-carboxamide (0.77 g, 2.14 mmol) in DMF (25 mL) is added zinc cyanide (0.26 g, 2.20 mmol), and tetrakis(triphenylphosphine)palladium (0) (0.25 g, 0.21 mmol). The resulting suspension is stirred at 95° C. for 48 h, then filtered through a pad of celite. The residue is purified using preparative chromatography (carried out on a Chiral OD column using a 40% IPA/heptanes each containing 0.1% diethylamine) to give a pale yellow oil that is salted with d-tartaric acid and crystallized from EtOH/Et2O to give a pale yellow solid. Yield 47%. HRMS (FAB) calcd for C16H17N5O+H 296.1511, found 296.1520.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06858613B2
出典データセットuspto-grants-2005_02
ORD IDord-35777fbdf51d4a96b2a0653b70a174ab
出典メモuspto-grants-2005_02