반응식
C(O[C:4](=[O:18])[CH2:5][CH2:6][NH:7][C:8]([O:10][CH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)=[O:9])C.[Li+].C[Si]([N-][Si](C)(C)C)(C)C.[CH:29]1([NH:34][C:35]2[C:40]([CH:41]=O)=[CH:39][N:38]=[C:37]([S:43][CH3:44])[N:36]=2)[CH2:33][CH2:32][CH2:31][CH2:30]1>O1CCCC1.C(OCC)(=O)C.O>[CH2:11]([O:10][C:8](=[O:9])[NH:7][CH2:6][C:5]1[C:4](=[O:18])[N:34]([CH:29]2[CH2:33][CH2:32][CH2:31][CH2:30]2)[C:35]2[N:36]=[C:37]([S:43][CH3:44])[N:38]=[CH:39][C:40]=2[CH:41]=1)[C:12]1[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=1참가 물질
반응물 3
생성물 1
시약·촉매·용매 3
실험 절차
3-Benzyloxycarbonylamino-propionic acid ethyl ester (6.68 g, 26.58 mmol) was dissolved in tetrahydrofuran (40 mL) to which LiHMDS (28 mL, 28 mmol, 1.0 M in THF) was slowly added. 4-Cyclopentylamino-2-methylsulfanyl-pyrimidine-5-carbaldehyde (3.15 g, 13.29 mmol) was then added neat and the reaction mixture was brought to reflux for 7 hours. The reaction mixture was diluted with ethyl acetate and water, the layers separated, the organic layer dried over MgSO4 and the solvent evaporated to give a crude oil. The crude oil was purified by silica gel chromatography to give (8-cyclopentyl-2-methylsulfanyl-7-oxo-7,8-dihydro-pyrido[2,3-d]pyrimidin-6-ylmethyl)-carbamic acid benzyl ester as pale yellow waxy solid (1.67 g, 29.6%). 1H NMR δ(400 MHz, CDCl3) 8.57 (s, 1H), 7.56 (s, 1H), 7.26-7.36 (m, 5H), 5.93 (m, 1H), 5.56 (t, J=6.1 Hz, 1H), 5.08 (s, 2H), 4.25 (d, J=6.2 Hz, 2H), 2.60 (s, 3H), 2.30 (m, 2H), 2.05 (m, 2H), 1.86 (m, 2H), 1.69 (m, 2H).
후처리
- additionwas slowly added
- temperatureto reflux for 7 hours
- customthe layers separated
- dry with materialthe organic layer dried over MgSO4
- customthe solvent evaporated
- customto give a crude oil
- customThe crude oil was purified by silica gel chromatography
출처 및 근거
- ORD 기록
- ord-95e396a5a27043bc9ea4509f4ace4671
- 출처 데이터셋
- uspto-grants-2008_11
- 특허 번호
- US07456168B2
연결된 노트
불러오는 중…