Triethylamine → Methyl cis-1-(2,4-Dimethoxybenzyl)-3-phenoxyacetamido-4-oxo-2-azetidinecarboxylate

HRID 127892

反応式

HRID 127892 の反応式
[CH3:1][O:2][C:3]1[CH:19]=[C:18]([O:20][CH3:21])[CH:17]=[CH:16][C:4]=1[CH2:5][N:6]1[C:9](=[O:10])[C@H:8]([NH2:11])[C@@H:7]1[C:12]([O:14][CH3:15])=[O:13].C(N(CC)CC)C.[O:29]([CH2:36][C:37](Cl)=[O:38])[C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1>C(Cl)Cl.CCOCC>[CH3:1][O:2][C:3]1[CH:19]=[C:18]([O:20][CH3:21])[CH:17]=[CH:16][C:4]=1[CH2:5][N:6]1[C:9](=[O:10])[C@H:8]([NH:11][C:37](=[O:38])[CH2:36][O:29][C:30]2[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=2)[C@@H:7]1[C:12]([O:14][CH3:15])=[O:13]

参加物

6

反応物 3

HCID 8471TriethylamineHCID 69703Phenoxyacetyl chlorideHCID 18632686Methyl cis-1-(2,4-Dimethoxybenzyl)-3-amino-4-oxoazetidine-2-carboxylate

生成物 1

HCID 70577439Methyl cis-1-(2,4-Dimethoxybenzyl)-3-phenoxyacetamido-4-oxo-2-azetidinecarboxylate収率 84%

試薬・触媒・溶媒 2

HCID 3283Diethyl Ether溶媒HCID 6344Dichloromethane溶媒2 回

実験手順

The crude amine prepared in Example 2 from 10 g of the azido precursor is taken up in 100 ml of anhydrous methylene dichloride and is cooled to 0° in an ice bath. To this solution is added 4.32 ml (0.0312 mol) of triethylamine followed by the slow addition of a solution of 5.32 g (0.0312 mol) of phenoxyacetyl chloride in 40 ml of methylene dichloride. The mixture is stirred at 0° for 1 hr. then poured into a separatory funnel and extracted successively with water, aqueous HCl, aqueous NaHCO3, brine and is dried over anhydrous magnesium sulfate. After filtration the solvent is removed in vacuo to give a yellow solid. This material is partially dissolved in ether, cooled to -25°, and filtered to afford 11.2 g (84%) of the title product as a white solid which is one spot on tlc: benzene-ethyl acetate (1:1), silica gel, Rf 0.38. An analytical sample, mp 115.5°-116.0°, is obtained by recrystallization from ethyl acetate-hexane.

後処理

  1. temperatureis cooled to 0° in an ice bath
  2. additionthen poured into a separatory funnel
  3. extractionextracted successively with water, aqueous HCl, aqueous NaHCO3, brine
  4. dry with materialis dried over anhydrous magnesium sulfate
  5. filtrationAfter filtration the solvent
  6. customis removed in vacuo
  7. customto give a yellow solid
  8. temperaturecooled to -25°
  9. filtrationfiltered

出典と根拠

ORDレコード
ord-f003fc53ffc94e068a6b49df21ae3ee1
出典データセット
uspto-grants-1981_03
特許番号
US04257947

関連ノート

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