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Cl.[F:2][C:3]([F:17])([F:16])[C:4]1[CH:5]=[C:6]([N:10]2[CH2:14][CH2:13][C:12]([NH2:15])=[N:11]2)[CH:7]=[CH:8][CH:9]=1.C(N(CC)CC)C.ClC1C(=O)C(C#N)=C(C#N)C(=O)C=1Cl.Cl>O1CCOCC1>[F:17][C:3]([F:2])([F:16])[C:4]1[CH:5]=[C:6]([N:10]2[CH:14]=[CH:13][C:12]([NH2:15])=[N:11]2)[CH:7]=[CH:8][CH:9]=1참가 물질
실험 절차
To a solution of 1-(3-trifluoromethyl-phenyl)-4,5-dihydro-1H-pyrazol-3-ylamine hydrochloride salt (200 mg, 0.88 mmol) (Example 3A) in dioxane (50 mL) was added triethylamine (0.069 mL, 0.88 mmol) followed by 2,3-dichloro-5,6-dicyano-p-benzoquinone (DDQ) (200 mg, 0.88 mmol). The mixture was stirred at room temperature for 24 h and then poured onto dichloromethane. 2N hydrochloric acid was added and the organics extracted with 2N hydrochloric acid (3×50 mL). The acid layer was basified with 10N potassium hydroxide and extracted with dichloromethane (3×50 mL). The combined organics were dried (Na2SO4), filtered and evaporated to dryness. The residue dissolved in diethyl ether and 1M hydrochloric acid in diethyl ether was added to form a brown solid which was collected and dried (171 mg, 86%). MS (ES) m/z: 228.1 [M+H].
후처리
- additionpoured onto dichloromethane
- extractionthe organics extracted with 2N hydrochloric acid (3×50 mL)
- extractionextracted with dichloromethane (3×50 mL)
- dry with materialThe combined organics were dried (Na2SO4)
- filtrationfiltered
- customevaporated to dryness
- dissolutionThe residue dissolved in diethyl ether
- addition1M hydrochloric acid in diethyl ether was added
- customto form a brown solid which
- customwas collected
- customdried (171 mg, 86%)
출처 및 근거
- ORD 기록
- ord-cbf8e473c0364d45bc73ff649687c3b1
- 출처 데이터셋
- uspto-grants-2009_01
- 특허 번호
- US07482469B2
연결된 노트
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