Water → [2-(2-Bromo-4,5-difluorobenzyloxy)ethyl]dimethylamine
反応式
[Br:1][C:2]1[CH:15]=[C:14]([F:16])[C:13]([F:17])=[CH:12][C:3]=1[CH2:4][O:5][CH2:6][CH2:7]CN(C)C.C(=O)([O-])[O-].[K+].[K+].O.N[C:26]1N=C(C(N2CC3C(=CC=CC=3)C2)=O)C2[C:28](=CC=C(B3OC(C)(C)C(C)(C)O3)C=2)[N:27]=1>C(O)C.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2]>[Br:1][C:2]1[CH:15]=[C:14]([F:16])[C:13]([F:17])=[CH:12][C:3]=1[CH2:4][O:5][CH2:6][CH2:7][N:27]([CH3:28])[CH3:26]参加物
7
反応物 4
生成物 1
試薬・触媒・溶媒 2
反応条件
- 温度
- 120 °C
実験手順
88 mg of [3-(2-bromo-4,5-difluorobenzyloxy)propyl]dimethylamine, 80 mg of potassium carbonate, 5 μl of water and 12 mg of [1,1′-bis(diphenylphosphino)ferrocene]palladium(II) dichloride are added to a solution of 150 mg of [2-amino-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinazolin-4-yl]-(1,3-dihydroisoindol-2-yl)methanone in 2 ml of ethanol under argon. The mixture is heated at 120° C. for 60 min. The solid is subsequently filtered off through kieselguhr with suction, and the filtrate is evaporated to dryness in vacuo. The residue is dissolved in 1 ml of DMSO and chromatographed by means of preparative HPLC (Agilent). The product fractions obtained are subsequently evaporated and freeze-dried.
後処理
- filtrationThe solid is subsequently filtered off through kieselguhr with suction
- customthe filtrate is evaporated to dryness in vacuo
- dissolutionThe residue is dissolved in 1 ml of DMSO
- customchromatographed by means of preparative HPLC (Agilent)
- customThe product fractions obtained
- customare subsequently evaporated
- customfreeze-dried
出典と根拠
- ORDレコード
- ord-5e68aaf9068c484498d6a0125a443f18
- 出典データセット
- uspto-grants-2014_07
- 特許番号
- US08791129B2
反応ノート
読み込み中…