Hydrochloric Acid → 1,3-dihydro-1-(3-hydroxypropyl)-5-(trifluoromethyl)-2H-benzimidazol-2-one

HRID 46843

反応式

HRID 46843 の反応式
[NH2:1][C:2]1[CH:7]=[C:6]([C:8]([F:11])([F:10])[F:9])[CH:5]=[CH:4][C:3]=1[NH:12][CH2:13][CH2:14][CH2:15][OH:16].Cl.[O-:18][C:19]#N.[K+]>O>[OH:16][CH2:15][CH2:14][CH2:13][N:12]1[C:3]2[CH:4]=[CH:5][C:6]([C:8]([F:10])([F:11])[F:9])=[CH:7][C:2]=2[NH:1][C:19]1=[O:18]

参加物

5

実験手順

To a stirred mixture of 21 parts of 3-{[2-amino-4-(trifluoromethyl)phenyl]amino}-1-propanol and 100 parts of water are added 14.4 parts of hydrochloric acid solution. The whole is stirred for 10 minutes at room temperature. After cooling to 0°-10° C., there is added dropwise a solution of 18 parts of potassium cyanate in 50 parts of water. Upon completion, stirring is continued for 2 hours. The precipitated product is filtered off and dried. Then it is melted and the melt is stirred for 10 minutes. After cooling, it is dissolved in trichloromethane while heating. The solution is filtered and the product is allowed to crystallize from the filtrate. It is filtered off and dried, yielding 8 parts (34%) of 1,3-dihydro-1-(3-hydroxypropyl)-5-(trifluoromethyl)-2H-benzimidazol-2-one.

後処理

  1. temperatureAfter cooling to 0°-10° C.
  2. stirringUpon completion, stirring
  3. waitis continued for 2 hours
  4. filtrationThe precipitated product is filtered off
  5. customdried
  6. stirringthe melt is stirred for 10 minutes
  7. temperatureAfter cooling
  8. dissolutionit is dissolved in trichloromethane
  9. temperaturewhile heating
  10. filtrationThe solution is filtered
  11. customto crystallize from the filtrate
  12. filtrationIt is filtered off
  13. customdried

出典と根拠

ORDレコード
ord-c7824292522f4497a8640ecf1cdb2402
出典データセット
uspto-grants-1979_11
特許番号
US04175129

関連ノート

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