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Dimethyl Sulfoxide → ethyl 3-{[(2R)-2-(4,5-diphenyloxazol-2-yl)-4-oxopyrrolidin-1-yl]methyl}phenoxyacetate

HRID 431763
ノート
印刷プレビュー

反応式

HRID 431763 の反応式
C(Cl)(=O)C(Cl)=O.CS(C)=O.[C:11]1([C:17]2[N:18]=[C:19]([C@H:28]3[CH2:32][C@@H:31]([OH:33])[CH2:30][N:29]3[CH2:34][C:35]3[CH:36]=[C:37]([CH:45]=[CH:46][CH:47]=3)[O:38][CH2:39][C:40]([O:42][CH2:43][CH3:44])=[O:41])[O:20][C:21]=2[C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1.C(N(CC)CC)C>C(Cl)Cl.CCOC(C)=O>[C:11]1([C:17]2[N:18]=[C:19]([C@H:28]3[CH2:32][C:31](=[O:33])[CH2:30][N:29]3[CH2:34][C:35]3[CH:36]=[C:37]([CH:45]=[CH:46][CH:47]=3)[O:38][CH2:39][C:40]([O:42][CH2:43][CH3:44])=[O:41])[O:20][C:21]=2[C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 679Dimethyl SulfoxideHCID 8471TriethylamineHCID 65578Oxalyl chlorideHCID 11156247ethyl 3-{[(2R, 4R)-2-(4,5-diphenyloxazol-2-yl)-4-hydroxypyrrolidin-1-yl]methyl}phenoxyacetate

生成物 1

HCID 69997743ethyl 3-{[(2R)-2-(4,5-diphenyloxazol-2-yl)-4-oxopyrrolidin-1-yl]methyl}phenoxyacetate収率 80.9%

試薬・触媒・溶媒 2

HCID 6344Dichloromethane溶媒3 回HCID 8857Ethyl Acetate溶媒

実験手順

To a solution of oxalyl chloride (0.050 mL) in CH2Cl2 (10 mL) was added a solution of DMSO (0.061 mL) in CH2Cl2 (0.5 mL) keeping the temperature below −55° C., and stirred for 30 minutes. To the mixture was added a solution of ethyl 3-{[(2R, 4R)-2-(4,5-diphenyloxazol-2-yl)-4-hydroxypyrrolidin-1-yl]methyl}phenoxyacetate (238 mg) in CH2Cl2 (3 mL) at the same temperature, then stirred for 1 hour. To the reaction mixture was added triethylamine (0.27 mL), and warmed to room temperature over 30 minutes. After stirring at the same temperature for 30 minutes, the mixture was diluted with EtOAc, washed with water, saturated sodium hydrogen carbonate, water and brine, dried (MgSO4), evaporated. The residue was purified by silica gel column chromatography (hexane-EtOAc 2:1) to give ethyl 3-{[(2R)-2-(4,5-diphenyloxazol-2-yl)-4-oxopyrrolidin-1-yl]methyl}phenoxyacetate (191.8 mg).

後処理

  1. customthe temperature below −55° C.
  2. stirringstirred for 1 hour
  3. stirringAfter stirring at the same temperature for 30 minutes
  4. washwashed with water, saturated sodium hydrogen carbonate, water and brine
  5. dry with materialdried (MgSO4)
  6. customevaporated
  7. customThe residue was purified by silica gel column chromatography (hexane-EtOAc 2:1)

出典と根拠

ORDレコード
ord-00216b76535542de86ed6ab32301df54
出典データセット
uspto-grants-2003_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06660759B1

反応ノート

読み込み中…

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