Methyl iodide → 2'-chloro-9'-isopropyl-5'-methyl-8',9'-dihydrospiro[cyclopropane-1,7'-pyrimido[5,4-b][1,4]diazepin]-6'(5'H)-one
反応式
[Cl:1][C:2]1[N:3]=[CH:4][C:5]2[NH:6][C:7](=[O:18])[C:8]3([CH2:17][CH2:16]3)[CH2:9][N:10]([CH:13]([CH3:15])[CH3:14])[C:11]=2[N:12]=1.[CH3:19]I.[H-].[Na+]>CC(N(C)C)=O.C(Cl)Cl>[Cl:1][C:2]1[N:3]=[CH:4][C:5]2[N:6]([CH3:19])[C:7](=[O:18])[C:8]3([CH2:16][CH2:17]3)[CH2:9][N:10]([CH:13]([CH3:15])[CH3:14])[C:11]=2[N:12]=1参加物
反応物 3
生成物 1
試薬・触媒・溶媒 2
実験手順
To a solution of 2′-chloro-9′-isopropyl-8′,9′-dihydrospiro[cyclopropane-1,7′-pyrimido[5,4-b][1,4]diazepin]-6′(5′H)-one (Intermediate 209; 5.055 g, 19 mmol) in DMA (300 mL) was added methyl iodide (1.305 mL, 20.9 mmol), followed by sodium hydride (60% mineral oil dispersion; 814 mg, 20.33 mmol). The mixture was stirred at room temperature for 30 minutes. The DMA was removed in vacuo, then water (50 mL) was added. The product precipitated as a sticky gum, which turned into a solid on sonication. The solid was collected by filtration to give a brown powder. This material was dissolved in DCM and dried over sodium sulfate, then purified by column chromatography, eluting with 25% ethyl acetate in hexane, to yield the title compound as a white solid (3.73 g, 70%)
後処理
- customThe DMA was removed in vacuo
- additionwater (50 mL) was added
- customThe product precipitated as a sticky gum, which
- customturned into a solid on sonication
- filtrationThe solid was collected by filtration
- customto give a brown powder
- dry with materialdried over sodium sulfate
- custompurified by column chromatography
- washeluting with 25% ethyl acetate in hexane
出典と根拠
- ORDレコード
- ord-22475971552642b0bc68e649ed03699a
- 出典データセット
- uspto-grants-2010_05
- 特許番号
- US07709471B2
反応ノート
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