反応式
Cl[C:2]1[N:7]=[CH:6][C:5]([B:8]([OH:10])[OH:9])=[CH:4][N:3]=1.[NH:11]1[CH2:16][CH2:15][O:14][CH2:13][CH2:12]1.C(N(CC)CC)C>CCO>[N:11]1([C:2]2[N:7]=[CH:6][C:5]([B:8]([OH:10])[OH:9])=[CH:4][N:3]=2)[CH2:16][CH2:15][O:14][CH2:13][CH2:12]1参加物
反応条件
- 温度
- 80 °C
実験手順
A mixture of 2-chloropyrimidin-5-ylboronic acid (3 g, 19.0 mmol), morpholine (1.66 mL, 19 mmol) and triethylamine (1.67 mL, 19.19 mmol) in EtOH (20 mL) was stirred at 80° C. for 5 h. LCMS indicated completion of the reaction. The reaction mixture was concentrated in vacuo and the residue was taken up in ethanol (approximately 5 mL). Diethyl ether was added, and the triethylamine hydrochloride salt that crystallised out was filtered and discarded. The filtrate was concentrated in vacuo and water (approximately 10 mL) was added. The mixture was placed in a refrigerator for 1 h, after which time the resulting solid was filtered off, washed with the minimum amount of water and dried by suction, to give the title compound (2.7 g, 68%) as an off-white solid. δH (DMSO-d6) 8.64 (s, 2H), 8.08 (s, 2H), 3.73 (m, 4H), 3.65 (m, 4H). LCMS (ES+) 210 (M+H)+, RT 0.15 minutes.
後処理
- customcompletion of the reaction
- concentrationThe reaction mixture was concentrated in vacuo
- additionDiethyl ether was added
- customthe triethylamine hydrochloride salt that crystallised out
- filtrationwas filtered
- concentrationThe filtrate was concentrated in vacuo and water (approximately 10 mL)
- additionwas added
- waitThe mixture was placed in a refrigerator for 1 h
- filtrationafter which time the resulting solid was filtered off
- washwashed with the minimum amount of water
- customdried by suction
出典と根拠
- ORDレコード
- ord-5c52ba6cdeb14ff7836b76be3b9116a4
- 出典データセット
- uspto-grants-2016_04
- 特許番号
- US09309243B2
関連ノート
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