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2-Butyl-4-chloro-5-(hydroxymethyl)imidazole → 2-Butyl-1-[4-(2-carbomethoxybenzoyl)benzyl]-4-chloro-5-hydroxymethylimidazole

HRID 653918
ノート
印刷プレビュー

反応式

HRID 653918 の反応式
[CH2:1]([C:5]1[NH:6][C:7]([CH2:11][OH:12])=[C:8]([Cl:10])[N:9]=1)[CH2:2][CH2:3][CH3:4].C[O-].[Na+].Br[CH2:17][C:18]1[CH:35]=[CH:34][C:21]([C:22]([C:24]2[CH:33]=[CH:32][CH:31]=[CH:30][C:25]=2[C:26]([O:28][CH3:29])=[O:27])=[O:23])=[CH:20][CH:19]=1>CO.CN(C=O)C>[CH2:1]([C:5]1[N:6]([CH2:17][C:18]2[CH:19]=[CH:20][C:21]([C:22](=[O:23])[C:24]3[CH:33]=[CH:32][CH:31]=[CH:30][C:25]=3[C:26]([O:28][CH3:29])=[O:27])=[CH:34][CH:35]=2)[C:7]([CH2:11][OH:12])=[C:8]([Cl:10])[N:9]=1)[CH2:2][CH2:3][CH3:4]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 27356622-Butyl-4-chloro-5-(hydroxymethyl)imidazoleHCID 10942334Sodium MethoxideHCID 19012308Methyl 2-(4-(bromomethyl)benzoyl)benzoate

生成物 1

HCID 198152912-Butyl-1-[4-(2-carbomethoxybenzoyl)benzyl]-4-chloro-5-hydroxymethylimidazole収率 61.8%

試薬・触媒・溶媒 2

HCID 887Methanol溶媒
HCID 6228
Dimethylformamide
溶媒

実験手順

To a solution of 2-butyl-4-chloro-5-(hydroxymethyl)imidazole (11.12 g, 54 mmol, 1 eq) in 200 mL methanol was added dropwise a freshly prepared sodium methoxide solution (1.36 g Na, 59mmol, 1.1 eq in 50 mL MeOH). After stirring for 0.5 hours, the methanol was removed in vacuo and the resultant glass was dissolved in 200 mL DMF. To this mixture was added a solution of methyl 2-[4-(bromomethyl)benzoyl]benzoate (18.00 g, 59 mmol, 1.1 eq) in DMF and the entire contents was stirred overnight under N2 at room temperature. The solvent was then removed in vacuo and the residue dissolved in 500 mL ethyl acetate and 500 mL H2O. The layers were separated and the aqueous layer was extracted twice with 500 mL portions of ethyl acetate. The organic layers were dried and concentrated and the crude product flash chromatographed to separate the two regioisomers in 60:40 hexane/ethyl acetate over silica gel. The faster moving isomer was isolated to yield 14.72 g of a glassy solid. NWR (200 MHz, CDCl3) δ8.03 (d, 1H, J=7Hz); 7.67 (m, 4H); 7.36 (d, 1H, J=7Hz); 7.05 (d, 2H, J=7Hz); 5.28 (s, 2H); 4.43 (s, 2H); 3.63 (s, 3H); 2.53 (t, 2H, J=7Hz,); 1.60 (t of t, 2H, J=7,7Hz); 1.30 (t of q, 2H, J=7,7Hz); 0.87 (t, 3H, J=7Hz). Mass Calcd. for C25H26ClF3N4O5S: 586.1264. Found: 586.1285.

後処理

  1. customthe methanol was removed in vacuo
  2. dissolutionthe resultant glass was dissolved in 200 mL DMF
  3. stirringthe entire contents was stirred overnight under N2 at room temperature
  4. customThe solvent was then removed in vacuo
  5. dissolutionthe residue dissolved in 500 mL ethyl acetate
  6. customThe layers were separated
  7. extractionthe aqueous layer was extracted twice with 500 mL portions of ethyl acetate
  8. customThe organic layers were dried
  9. concentrationconcentrated
  10. customthe crude product flash chromatographed
  11. customto separate the two regioisomers in 60:40 hexane/ethyl acetate over silica gel
  12. customwas isolated

出典と根拠

ORDレコード
ord-af969166a28f464db9daf046b2958cf2
出典データセット
uspto-grants-1992_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05128355

反応ノート

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