2-Pyrrolidone → HCID 89579872, 화합물
반응식
[H-].[Na+].[NH:3]1[CH2:7][CH2:6][CH2:5][C:4]1=[O:8].Cl[CH2:10][C:11]1[N:12]=[C:13]([N:26]2[CH2:31][CH2:30][CH:29]([CH2:32][OH:33])[CH2:28][CH2:27]2)[C:14]2[C:19]([C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=3)=[CH:18][S:17][C:15]=2[N:16]=1>CN(C)C=O>[OH:33][CH2:32][CH:29]1[CH2:30][CH2:31][N:26]([C:13]2[C:14]3[C:19]([C:20]4[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=4)=[CH:18][S:17][C:15]=3[N:16]=[C:11]([CH2:10][N:3]3[CH2:7][CH2:6][CH2:5][C:4]3=[O:8])[N:12]=2)[CH2:27][CH2:28]1참가 물질
실험 절차
Sodium hydride (25 mg, 60% w/w in mineral oil) was added to a solution of 2-pyrrolidinone in dry N,N-dimethylformamide (2 mL) under a nitrogen atmosphere. The mixture was stirred for 10 min then [1-[2-(chloromethyl)-5-phenyl-thieno[2,3-d]pyrimidin-4-yl]-4-piperidyl]methanol (100 mg) was added. The mixture was stirred for 2 hr at room temperature. The solvent was evaporated and the residue was dissolved in ethyl acetate (10 mL) and water (10 mL). The layers were separated and the aqueous was extracted with ethyl acetate (2×10 mL). The combined organic layers were washed with brine (1×10 mL), dried (sodium sulfate), filtered and evaporated to give the target compound (96 mg) as a yellow solid. m/z [M+H]+ 424.0. Retention time 3.95 min (LCMS method+ve 6 min). It was used in the next reaction without purification.
후처리
- stirringThe mixture was stirred for 2 hr at room temperature
- customThe solvent was evaporated
- dissolutionthe residue was dissolved in ethyl acetate (10 mL)
- customThe layers were separated
- extractionthe aqueous was extracted with ethyl acetate (2×10 mL)
- washThe combined organic layers were washed with brine (1×10 mL)
- dry with materialdried (sodium sulfate)
- filtrationfiltered
- customevaporated
출처 및 근거
- ORD 기록
- ord-c4d63b1a195241739c7b5b4d15aaa5e3
- 출처 데이터셋
- uspto-grants-2016_03
- 특허 번호
- US09290511B2
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