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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 852455생성일: 2026년 10월 25일

Diisopropylamine → N-[4-[1-(phenylmethyl)-4-piperidinyl]phenyl]-[1,1'-biphenyl]-2-carboxamide

https://huagongshe.com/reaction/852455

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylamineHCID 7912—
반응물Thionyl ChlorideHCID 24386—
반응물o-Phenylbenzoic acidHCID 70357—
반응물4-[1-(Phenylmethyl)-4-piperidinyl]-benzenamineHCID 22499396—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물N-[4-[1-(phenylmethyl)-4-piperidinyl]phenyl]-[1,1'-biphenyl]-2-carboxamideHCID 22499413112%

반응 단계

[1,1′-Biphenyl]-2-carboxylic acid (0.25 mol) was dissolved in DCM (500 ml) and DMF (0.5 ml). Thionyl chloride (0.51 mol) was added dropwise. The mixture was stirred and refluxed for 1 hour under nitrogen flow. The solvent was evaporated. DCM (500 ml) was added twice. The solvent was evaporated twice. The residue was dissolved in DCM (200 ml) and then added dropwise at 0° C. to a mixture of 4-[1-(phenylmethyl)-4-piperidinyl]-benzenamine (0.25 mol) and N-(1-methylethyl)-2-propanamine (0.75 mol) in DCM (800 ml). The mixture was brought to room temperature and then stirred at room temperature overnight under nitrogen flow. The mixture was washed three times with water (800 ml). The organic layer was separated, dried, filtered and the solvent was evaporated, yielding 125 g of N-[4-[1-(phenylmethyl)-4-piperidinyl]phenyl]-[1,1′-biphenyl]-2-carboxamide (intermediate 18).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07253157B2
출처 데이터셋uspto-grants-2007_08
ORD IDord-3c5b4a952a3e4e38be826265506ff424
출처 메모uspto-grants-2007_08