3-(Trifluoromethyl)phenol → m-Trifluoromethylphenyl 1-amidino-4-piperidinepropionate hydrochloride
반응식
[ClH:1].[C:2]([N:5]1[CH2:10][CH2:9][CH:8]([CH2:11][CH2:12][C:13]([OH:15])=[O:14])[CH2:7][CH2:6]1)(=[NH:4])[NH2:3].[F:16][C:17]([F:26])([F:25])[C:18]1[CH:19]=[C:20](O)[CH:21]=[CH:22][CH:23]=1.C1(N=C=NC2CCCCC2)CCCCC1>N1C=CC=CC=1>[ClH:1].[C:2]([N:5]1[CH2:10][CH2:9][CH:8]([CH2:11][CH2:12][C:13]([O:15][C:22]2[CH:21]=[CH:20][CH:19]=[C:18]([C:17]([F:26])([F:25])[F:16])[CH:23]=2)=[O:14])[CH2:7][CH2:6]1)(=[NH:3])[NH2:4]참가 물질
실험 절차
A mixture of 4.0 g of 1-amidino-4-piperidinepropionic acid hydrochloride and 2.75 g of m-trifluoromethylphenol was suspended in 27 ml of dry pyridine. To the suspension was added 3.5 g of dicyclohexylcarbodiimide, and the resulting mixture was stirred at room temperature for 6 hours. After removal of any insoluble materials, the solvent was removed. The residue was washed with ether, dissolved in chloroform and then stirred. After removal of any insoluble materials, the filtrate was washed twice with a saturated sodium chloride solution and then dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure to obtain 4.0 g (yield: 62.0%) of m-trifluoromethylphenyl 1-amidino-4-piperidinepropionate hydrochloride as colorless crystals having a melting point of 97° to 100° C.
후처리
- customAfter removal of any insoluble materials
- customthe solvent was removed
- washThe residue was washed with ether
- dissolutiondissolved in chloroform
- stirringstirred
- customAfter removal of any insoluble materials
- washthe filtrate was washed twice with a saturated sodium chloride solution
- dry with materialdried over anhydrous sodium sulfate
- customThe solvent was removed under reduced pressure
출처 및 근거
- ORD 기록
- ord-cd0940ffb03942e794163208124b35a5
- 출처 데이터셋
- uspto-grants-1984_02
- 특허 번호
- US04433152
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