Hydrochloric Acid → 3-(4-chloro-2-fluoro-5-isopropoxyphenyl)-1,5,6,7-tetrahydro-2H-cyclopenta[d]pyrimidine-2,4(3H)-dione

HRID 1722937ノート

反応式

HRID 1722937 の反応式
[Cl:1][C:2]1[C:7]([O:8][CH:9]([CH3:11])[CH3:10])=[CH:6][C:5]([NH:12][C:13](=[O:25])[NH:14][C:15]2[CH2:19][CH2:18][CH2:17][C:16]=2[C:20](OCC)=[O:21])=[C:4]([F:26])[CH:3]=1.C[O-].[Na+].Cl>CO>[Cl:1][C:2]1[C:7]([O:8][CH:9]([CH3:11])[CH3:10])=[CH:6][C:5]([N:12]2[C:20](=[O:21])[C:16]3[CH2:17][CH2:18][CH2:19][C:15]=3[NH:14][C:13]2=[O:25])=[C:4]([F:26])[CH:3]=1

参加物

5

反応物 3

HCID 313Hydrochloric AcidHCID 10942334Sodium MethoxideHCID 20026019HCID 20026019、化合物

生成物 1

HCID 200260343-(4-chloro-2-fluoro-5-isopropoxyphenyl)-1,5,6,7-tetrahydro-2H-cyclopenta[d]pyrimidine-2,4(3H)-dione

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

A suspension of 6.0 g of ethyl 2-[3-(4-chloro-2-fluoro-5-isopropoxyphenyl)ureido]-1-cyclopentenecarboxylate in 100 ml of absolute methanol is treated while stirring at room temperature with 7.8 ml of 2N sodium methylate solution and the reaction mixture is stirred for 2 hours. The solution is treated with 7.8 ml of 2N hydrochloric acid and evaporated to dryness. The residue is dissolved in 200 ml of ethyl acetate and the solution is washed with water, dried over anhydrous sodium sulphate and evaporated to dryness under reduced pressure. The residue is recrystallized from methylene chloride/diethyl ether. There is obtained 3-(4-chloro-2-fluoro-5-isopropoxyphenyl)-1,5,6,7-tetrahydro-2H-cyclopenta[d]pyrimidine-2,4(3H)-dione, m.p. 215°-217° C.

後処理

  1. additionis treated
  2. customevaporated to dryness
  3. dissolutionThe residue is dissolved in 200 ml of ethyl acetate
  4. washthe solution is washed with water
  5. dry with materialdried over anhydrous sodium sulphate
  6. customevaporated to dryness under reduced pressure
  7. customThe residue is recrystallized from methylene chloride/diethyl ether

出典と根拠

ORDレコード
ord-b577cd24214e4fb2af649640b720ec14
出典データセット
uspto-grants-1989_08
特許番号
US04859229

反応ノート

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