Dimethylformamide → HCID 131715264、化合物

HRID 2309640ノート

反応式

HRID 2309640 の反応式
Br[CH2:2][CH2:3][O:4][C:5]1[N:9]([CH3:10])N=NN=1.[F:11][C:12]1[CH:17]=[CH:16][C:15]([CH2:18][N:19]2[C:23]3[CH:24]=[CH:25][CH:26]=[CH:27][C:22]=3[N:21]=[C:20]2[CH2:28][CH:29]2[CH2:34][CH2:33][N:32]([CH2:35]CN)[CH2:31][CH2:30]2)=[CH:14][CH:13]=1.[C:38](=[O:41])([O-:40])[O-:39].[Na+].[Na+].CN(C)C=[O:47]>O>[C:5]([OH:4])(=[O:47])[C:38]([OH:40])=[O:41].[F:11][C:12]1[CH:17]=[CH:16][C:15]([CH2:18][N:19]2[C:23]3[CH:24]=[CH:25][CH:26]=[CH:27][C:22]=3[N:21]=[C:20]2[CH2:28][CH:29]2[CH2:34][CH2:33][N:32]([CH2:35][CH2:10][N:9]3[CH2:2][CH2:3][O:4][C:5]3=[O:39])[CH2:31][CH2:30]2)=[CH:14][CH:13]=1

参加物

6

反応物 4

HCID 6228DimethylformamideHCID 10340Sodium CarbonateHCID 14518041HCID 14518041、化合物HCID 14518104HCID 14518104、化合物

生成物 1

HCID 131715264HCID 131715264、化合物収率 13%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

A mixture of 4 parts of 5-(2-bromoethoxy)-1-methyl-1H-tetrazole, 5.5 parts of 4-[[1-[(4-fluorophenyl)methyl]-1H-benzimdazol-2-yl]methyl]-1-piperidineethanamine, 2.3. parts of sodium carbonate and 45 parts of N,N-dimethylformamide was stirred overnight at 70° C. The reaction mixture was poured into water. The product was extracted with 4-methyl-2-pentanone. The extract was dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was converted into the ethanedioate salt in ethanol. The salt was filtered off and dried, yielding 1.3 parts (13%) of 3-[2-[4-[[1-[(4-fluorophenyl)methyl]-1H-benzimidazol-2-yl]methyl]-1-piperidinyl]ethyl]2-oxazolidinone ethanedioate(2:5); mp. 147.9° C. (385).

後処理

  1. extractionThe product was extracted with 4-methyl-2-pentanone
  2. customThe extract was dried
  3. filtrationfiltered
  4. customevaporated
  5. customThe residue was purified by column chromatography over silica gel using
  6. additiona mixture of trichloromethane and methanol (95:5 by volume) as eluent
  7. customThe pure fractions were collected
  8. customthe eluent was evaporated
  9. filtrationThe salt was filtered off
  10. customdried

出典と根拠

ORDレコード
ord-ac0cfbb685bc4e5183eb8ae6b0368042
出典データセット
uspto-grants-1987_09
特許番号
US04695575

反応ノート

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