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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1638782생성일: 2026년 10월 27일

Hydrochloric Acid → 1-(5,6-dimethoxy-1H-inden-2-ylcarbonyl)-4-(3,4,5-trimethoxybenzyl)piperazine hydrochloride

https://huagongshe.com/reaction/1638782

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Diethyl cyanophosphonateHCID 76257—
반응물5,6-dimethoxy-1H-indene-2-carboxylic AcidHCID 10376162—
반응물1-[(3,4,5-Trimethoxyphenyl)methyl]piperazine;dihydrochlorideHCID 12828501—
용매EthanolHCID 702—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
용매TriethylamineHCID 8471—
생성물1-(5,6-dimethoxy-1H-inden-2-ylcarbonyl)-4-(3,4,5-trimethoxybenzyl)piperazine hydrochlorideHCID 1984119479%

반응 단계

Diethyl phosphorocyanidate (0.9 g) is added dropwise to an ice-cooling mixture consisting of 5,6-dimethoxy-1H-indene-2-carboxylic acid (0.8 g), 1-(3,4,5-trimethyoxybenzyl)piperazine dihydrochloride (1.3 g), triethylamine (2 ml) and N,N-dimethylformamide (12 ml) with stirring. The whole mixture is stirred at room temperature for two hours and water is added. The mixture is extracted with ethyl acetate. The extract solution is washed with water, dried and then concentrated under reduced pressure. The residue is purified by silica gel column chromatography (ethyl acetate:hexane:acetone=12:8:5) to give an oily product. This product is converted to the hydrochloride in ethanol to afford 1-(5,6-dimethoxy-1H-inden-2-ylcarbonyl)-4-(3,4,5-trimethoxybenzyl)piperazine hydrochloride (1.45 g) as colorless scales, m.p. 245°-250° C. (decomp.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04880809
출처 데이터셋uspto-grants-1989_11
ORD IDord-a5a0f17cc8594deda3d7640ee42b160e
출처 메모uspto-grants-1989_11