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Water → HCID 14551615、化合物

HRID 846527
ノート
印刷プレビュー

反応式

HRID 846527 の反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[CH2:12][NH:11][N:10]=[N:9]2)=[C:4]([F:13])[CH:3]=1.[F:14][CH2:15][CH2:16][CH2:17]Br.C(=O)([O-])[O-:20].[K+].[K+].O>CN(C)C=O>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[C:12](=[O:20])[N:11]([CH2:17][CH2:16][CH2:15][F:14])[N:10]=[N:9]2)=[C:4]([F:13])[CH:3]=1
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 4

HCID 962WaterHCID 11430Potassium CarbonateHCID 67699Propane, 1-bromo-3-fluoro-HCID 1785058281-(4-chloro-2-fluorophenyl)-1,4-dihydro-5H-tetrazole

生成物 1

HCID 14551615HCID 14551615、化合物

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

A stirred solution of 4.7 grams (0.22 mole) of 1-(4-chloro-2-fluorophenyl)-1,4-dihydro-5H-tetrazole, 4.0 grams (0.028 mole) of 3-fluoropropyl bromide and 4.0 grams (0.028 mole) of potassium carbonate in 60 ml of dimethylformamide was heated at 60° C. for 16 hours. The reaction mixture was poured into water and the mixture extracted with diethyl ether. The combined ether extract was dried with magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure to a residue. The residue was dissolved in methylene chloride and passed through a pad of silica gel. The eluate was concentrated under reduced pressure to yield 3.5 grams of 1-(4-chloro-2-fluorophenyl-1,4-dihydro-4-(3-fluoropropyl)-5H-tetrazol-5-one; m.p. 62°-63° C. The reaction was repeated several times.

後処理

  1. extractionthe mixture extracted with diethyl ether
  2. extractionThe combined ether extract
  3. dry with materialwas dried with magnesium sulfate
  4. filtrationfiltered
  5. concentrationThe filtrate was concentrated under reduced pressure to a residue
  6. dissolutionThe residue was dissolved in methylene chloride
  7. concentrationThe eluate was concentrated under reduced pressure

出典と根拠

ORDレコード
ord-dde8f128ab5f4243b99e887e2d7e3387
出典データセット
uspto-grants-1992_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05136868

反応ノート

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