Cyclopropylamine → HCID 86725119、化合物
反応式
[Cl:1][C:2]1[N:7]=[C:6]([C:8]([OH:10])=O)[CH:5]=[CH:4][N:3]=1.CC[N:13]([CH:17]([CH3:19])[CH3:18])C(C)C.C1CN([P+](ON2N=NC3C=CC=CC2=3)(N2CCCC2)N2CCCC2)CC1.F[P-](F)(F)(F)(F)F.C1(N)CC1>O1CCOCC1>[Cl:1][C:2]1[N:7]=[C:6]([C:8]([NH:13][CH:17]2[CH2:19][CH2:18]2)=[O:10])[CH:5]=[CH:4][N:3]=1参加物
実験手順
2-Chloropyrimidine-4-carboxylic acid (0.516 g, 3.25 mmol) (Maybridge Chemicals, Maybridge, UK), DIPEA (0.94 mL, 5.42 mmol) and PyBop (1.69 g, 3.25 mmol) were weighed into a 150 mL RBF and dissolved in dioxane (15 mL). The solution was stirred at RT, then cooled to 0° C., and stirred for 5 min. Cyclopropylamine (0.38 mL, 5.42 mmol) was added, and the solution was stirred at 0° C. for 1 h. The mixture became solid. Additional dioxane was added (6 mL), the flask was removed from the ice bath and the contents were stirred at RT for 68 h. EtOAc was added and the mixture was washed with water (75 mL), 1 N NaOH (75 mL) and brine (75 mL). The crude material was purified by flash chromatography using an ISCO Combiflash Rf(25 g Thomson Single Step silica gel column; 20-100% EtOAc in hexanes) to afford 2-chloro-N-cyclopropylpyrimidine-4-carboxamide (0.139 g, 0.703 mmol, 25.9% yield) as a yellow oil. MS (ESI, pos. ion) m/z: 197.9 (M+H)+.
後処理
- temperaturecooled to 0° C.
- stirringstirred for 5 min
- stirringthe solution was stirred at 0° C. for 1 h
- customthe flask was removed from the ice bath
- stirringthe contents were stirred at RT for 68 h
- additionEtOAc was added
- washthe mixture was washed with water (75 mL), 1 N NaOH (75 mL) and brine (75 mL)
- customThe crude material was purified by flash chromatography
出典と根拠
- ORDレコード
- ord-43c06c15d36b49f98874cad252f64495
- 出典データセット
- uspto-grants-2016_04
- 特許番号
- US09321756B2
反応ノート
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