Sodium Hydroxide → N-[1-(2-aminoethyl)-4-piperidinyl]-1-(2-thienylmethyl)-1H-benzimidazol-2-amine

HRID 1493909ノート

反応式

HRID 1493909 の反応式
[H-].[Al+3].[Li+].[H-].[H-].[H-].Cl.FC1C=CC(CNC2C=NC=CC=2[N+]([O-])=O)=CC=1.[S:26]1[CH:30]=[CH:29][CH:28]=[C:27]1[CH2:31][N:32]1[C:36]2[CH:37]=[CH:38][CH:39]=[CH:40][C:35]=2[N:34]=[C:33]1[NH:41][CH:42]1[CH2:47][CH2:46][N:45]([CH2:48][C:49]#[N:50])[CH2:44][CH2:43]1.[OH-].[Na+]>O1CCCC1.O>[NH2:50][CH2:49][CH2:48][N:45]1[CH2:46][CH2:47][CH:42]([NH:41][C:33]2[N:32]([CH2:31][C:27]3[S:26][CH:30]=[CH:29][CH:28]=3)[C:36]3[CH:37]=[CH:38][CH:39]=[CH:40][C:35]=3[N:34]=2)[CH2:43][CH2:44]1

参加物

7

実験手順

To a stirred mixture of 2.5 parts of lithium aluminum hydride and 225 parts of tetrahydrofuran was added dropwise a solution of 13 parts of 4-[[1-(2-thienylmethyl)-1H-benzimidazol-2-yl]amino]-1-piperidineacetonitrile in tetrahydrofuran under nitrogen atmosphere. Upon completion, stirring was continued for 3 hours at reflux. The reaction mixture was cooled in an ice bath and decomposed by the successive additions of 2.5 parts of water, 7.5 parts of a sodium hydroxide solution 15% and 7.5 parts of water. The whole was filtered over Hyflo and the filtrate was evaporated. The residue was crystallized from acetonitrile, yielding 9.5 parts (72%) of N-[1-(2-aminoethyl)-4-piperidinyl]-1-(2-thienylmethyl)-1H-benzimidazol-2-amine; mp. 137.1° C. (intermediate 108).

後処理

  1. temperatureat reflux
  2. temperatureThe reaction mixture was cooled in an ice bath
  3. filtrationThe whole was filtered over Hyflo
  4. customthe filtrate was evaporated
  5. customThe residue was crystallized from acetonitrile

出典と根拠

ORDレコード
ord-a7a980577dd2437ca41132dc573953f9
出典データセット
uspto-grants-1991_06
特許番号
US05025014

反応ノート

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