Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1375950생성일: 2026년 10월 25일
Diisopropylamine → N-[4-[1-(phenylmethyl)-4-piperidinyl]phenyl]-[1,1'-biphenyl]-2-carboxamide
https://huagongshe.com/reaction/1375950
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Diisopropylamine | HCID 7912 | — |
| 반응물 | Thionyl Chloride | HCID 24386 | — |
| 반응물 | o-Phenylbenzoic acid | HCID 70357 | — |
| 반응물 | 4-[1-(Phenylmethyl)-4-piperidinyl]-benzenamine | HCID 22499396 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | N-[4-[1-(phenylmethyl)-4-piperidinyl]phenyl]-[1,1'-biphenyl]-2-carboxamide | HCID 22499413 | 112% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07169796B2 |
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| 출처 데이터셋 | uspto-grants-2007_01 |
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| ORD ID | ord-a0db70bc6330407498025c3a96bc8379 |
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| 출처 메모 | uspto-grants-2007_01 |
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