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HRID 2267117作成日:2026年10月25日

Norcamphor → 1'-(bicyclo[2.2.1]heptan-2-yl)-N-(pentan-3-yl)spiro[indene-1,4'-piperidine]-3-carboxamide

https://huagongshe.com/reaction/2267117

反応式

関与物質

役割名称HCID仕込み量
反応物NorcamphorHCID 449588—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物N-(pentan-3-yl)spiro[indene-1,4'-piperidine]-3-carboxamideHCID 25012980—
触媒Titanium isopropoxideHCID 11026—
溶媒1,1-DichloroethaneHCID 6365—
生成物1'-(bicyclo[2.2.1]heptan-2-yl)-N-(pentan-3-yl)spiro[indene-1,4'-piperidine]-3-carboxamideHCID 25012003—

反応手順

A mixture of (F2) (0.020 g, 0.05 mmol), titanium (IV) isopropoxide (0.045 mL, 0.15 mmol) and (1R,4S)-bicyclo[2.2.1]heptan-2-one (3 eq) was stirred at room temperature for 18 h in dichloroethane (0.5 mL). Sodium triacetoxyborohydride (0.011 g, 0.050 mmol) was added and the mixture stirred at room temperature for 1 h. The solvent was evaporated and 6N NaOH (0.5 mL) and methanol (1 mL) was added and then triturated to give a white solid that was washed with methanol (1 mL) and EtOAc (1 mL). The filtrate was concentrated under reduced pressure to afford the crude product which was purified by reverse phase preparative HPLC to afford 1′-(bicyclo[2.2.1]heptan-2-yl)-N-(pentan-3-yl)spiro[indene-1,4′-piperidine]-3-carboxamide (Compound No. 14) (0.013 g). LC/MS (10-90% over 3 min with 0.9% FA) m/z 324.1 (M+1), retention time 2.2 minutes.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07858790B2
出典データセットuspto-grants-2010_12
ORD IDord-c49b317282534b7ea482afc586683ca0
出典メモuspto-grants-2010_12