Potassium Carbonate → 2-Fluoro-6-(1h-imidazol-2-yl)pyridine

HRID 916637ノート

反応式

HRID 916637 の反応式
[CH2:1]([C:4]1[C:5]([Cl:12])=[N:6][CH:7]=[N:8][C:9]=1[CH2:10]Br)[CH2:2][CH3:3].C(C1C(Cl)=NC=NC=1CCl)CC.[F:25][C:26]1[N:31]=[C:30]([C:32]2[NH:33][CH:34]=[CH:35][N:36]=2)[CH:29]=[CH:28][CH:27]=1.C([O-])([O-])=O.[K+].[K+]>CN(C=O)C>[F:25][C:26]1[N:31]=[C:30]([C:32]2[NH:36][CH:35]=[CH:34][N:33]=2)[CH:29]=[CH:28][CH:27]=1.[Cl:12][C:5]1[N:6]=[CH:7][N:8]=[C:9]([CH2:10][N:36]2[CH:35]=[CH:34][N:33]=[C:32]2[C:30]2[CH:29]=[CH:28][CH:27]=[C:26]([F:25])[N:31]=2)[C:4]=1[CH2:1][CH2:2][CH3:3]

参加物

7

反応物 4

HCID 11430Potassium CarbonateHCID 219192862-Fluoro-6-(1h-imidazol-2-yl)pyridineHCID 223131604-Bromomethyl-5-propyl-6-chloro-pyrimidineHCID 534265344-Chloro-6-(chloromethyl)-5-propylpyrimidine

生成物 2

HCID 219192862-Fluoro-6-(1h-imidazol-2-yl)pyridineHCID 223131636-Chloro-4-[2-(6-fluoro-pyridin-2-yl)-imidazol-1-ylmethyl]-5-propyl-pyrimidine

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

6-Fluoro-2-(1H-imidazol-2-yl)-pyridine is prepared as described in Example 16 of U.S. patent application Ser. No. 10/038,069, filed Dec. 12, 2001 and published as US 2003/0069257 on Apr. 10, 2003, which is hereby incorporated by reference at page 31 for its teaching regarding the synthesis of this compound. A mixture of 102 or 5-propyl-6-chloromethyl-4-chloro-pyrimidine (1 mmol of either), 6-fluoro-2-(1H-imidazol-2-yl)-pyridine (163 mg, 1 mmol) and K2CO3 (552 mg, 4 mmol) in DMF (6 ml) is stirred at room temperature overnight. The solvent is removed in vacuo and EtOAc (10 ml) and water (10 ml) are added to the residue. The layers are separated and the aqueous layer is extracted with EtOAc (10 ml). The combined extracts are washed with brine (10 ml), dried (Na2SO4) and evaporated. PTLC separation of the residue with 5% MeOH in CH2Cl2 provides the product (103) as a white solid.

後処理

  1. customthe synthesis of this compound
  2. customThe solvent is removed in vacuo and EtOAc (10 ml) and water (10 ml)
  3. additionare added to the residue
  4. customThe layers are separated
  5. extractionthe aqueous layer is extracted with EtOAc (10 ml)
  6. washThe combined extracts are washed with brine (10 ml)
  7. dry with materialdried (Na2SO4)
  8. customevaporated
  9. customPTLC separation of the residue with 5% MeOH in CH2Cl2

出典と根拠

ORDレコード
ord-c179f48f91c74431a810dec803063dad
出典データセット
uspto-grants-2007_09
特許番号
US07271170B2

反応ノート

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