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Triethylamine → N-{4-[6-(3,5-Dimethyl-benzoyl)-5-isopropyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-ylmethyl]-pyridin-2-yl}-acetamide

HRID 426150
ノート
印刷プレビュー

反応式

HRID 426150 の反応式
O[CH2:2][C:3]1[CH:8]=[CH:7][N:6]=[C:5]([NH:9][C:10](=[O:12])[CH3:11])[CH:4]=1.C(N(CC)CC)C.CS(Cl)(=O)=O.[CH3:25][C:26]1[CH:27]=[C:28]([CH:42]=[C:43]([CH3:45])[CH:44]=1)[C:29]([C:31]1[NH:36][C:35](=[O:37])[NH:34][C:33](=[O:38])[C:32]=1[CH:39]([CH3:41])[CH3:40])=[O:30].C(=O)([O-])[O-].[K+].[K+].[I-].[Li+]>C(Cl)(Cl)Cl.CN(C=O)C>[CH3:45][C:43]1[CH:42]=[C:28]([CH:27]=[C:26]([CH3:25])[CH:44]=1)[C:29]([C:31]1[N:36]([CH2:2][C:3]2[CH:8]=[CH:7][N:6]=[C:5]([NH:9][C:10](=[O:12])[CH3:11])[CH:4]=2)[C:35](=[O:37])[NH:34][C:33](=[O:38])[C:32]=1[CH:39]([CH3:41])[CH3:40])=[O:30]
参加物実験手順後処理出典と根拠反応ノート

参加物

9

反応物 6

HCID 8471TriethylamineHCID 11430Potassium CarbonateHCID 31297Methanesulfonyl chlorideHCID 66321Lithium iodideHCID 222565826-(3,5-Dimethyl-benzoyl)-5-isopropyl-1H-pyrimidine-2,4-dioneHCID 23151114N-(4-(hydroxymethyl)pyridin-2-yl)acetamide

生成物 1

HCID 66705547
N-{4-[6-(3,5-Dimethyl-benzoyl)-5-isopropyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-ylmethyl]-pyridin-2-yl}-acetamide
収率 38%

試薬・触媒・溶媒 2

HCID 6212Chloroform溶媒HCID 6228Dimethylformamide溶媒

実験手順

N-(4-Hydroxymethyl-pyridin-2-yl)-acetamide (166 mg, 1 mmol) was dissolved in chloroform (10 ml) and cooled in an ice bath under nitrogen atmosphere. With stirring, triethylamine (210 μl, 1.5 mmol) was added and methanesulfonyl chloride (90 μl, 1.2 mmol) was added dropwise. After stirring for 1.1 hr., the reaction mixture was washed with saturated aqueous sodium bicarbonate, dried with anhydrous magnesium sulfate, filtered, and evaporated in vacuo. The residue was further dried in high vacuo for ca. 20 min. and mixed with (20) (286 mg, 1 mmol), powdered anhydrous potassium carbonate (138 mg, 1 mmol), and lithium iodide (134 mg, 1 mmol). DMF (5 ml) was then added to the mixture at room temperature and stirred for ca. 4 hr. After evaporation of DMF, the residue was dissolved in methanol-chloroform (1:9) and filtered through celite pad. The filtrate was then evaporated in vacuo and the residue was purified by silica gel column chromatography (eluent, EA:hexanes (2:1)) to afford 165 mg (38%) a white solid. m.p. 244-245° C.; 1H NMR (200 MHz, CDCl3) δ 1.17 (3H, d, J=6.7 Hz), 1.24 (3H, d, J=6.7 Hz), 2.20-2.40 (10H, m), 4.70 (1H, d, J=17.1 Hz), 4.88 (1H, d, J=17.1 Hz), 6.82 (1H, d, J=5.3 Hz), 7.24 (1H, s), 7.42 (2H, s), 7.99 (1H, s), 8.30 (1H, d, J=5.3 Hz), 10.01 (1H, s), 12.44 (1H, s); m/z (EI) 434 (M+).

後処理

  1. temperaturecooled in an ice bath under nitrogen atmosphere
  2. stirringAfter stirring for 1.1 hr
  3. wash, the reaction mixture was washed with saturated aqueous sodium bicarbonate
  4. dry with materialdried with anhydrous magnesium sulfate
  5. filtrationfiltered
  6. customevaporated in vacuo
  7. customThe residue was further dried in high vacuo for ca. 20 min.
  8. stirringstirred for ca. 4 hr
  9. customAfter evaporation of DMF
  10. dissolutionthe residue was dissolved in methanol-chloroform (1:9)
  11. filtrationfiltered through celite pad
  12. customThe filtrate was then evaporated in vacuo
  13. customthe residue was purified by silica gel column chromatography (eluent, EA:hexanes (2:1))

出典と根拠

ORDレコード
ord-cf4f9885c31d4519a9baba305e5ee1a5
出典データセット
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08106064B2

反応ノート

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