Tin tetrachloride → HCID 178480624、化合物

HRID 392610

反応式

HRID 392610 の反応式
[N:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[NH:3][C:2]=1[CH2:10][C:11]([O:13]CC)=O.[NH2:16][C:17]1[CH:22]=[CH:21][C:20]([N:23]2[CH2:28][CH2:27][N:26]([CH3:29])[CH2:25][CH2:24]2)=[CH:19][C:18]=1[C:30]#[N:31].Cl[Sn](Cl)(Cl)Cl>ClCCCl>[CH3:29][N:26]1[CH2:25][CH2:24][N:23]([C:20]2[CH:21]=[CH:22][C:17]3[C:18](=[C:30]([NH2:31])[C:10]([C:11]([N:16]=3)=[O:13])=[C:2]3[NH:1][C:5]4[C:4](=[CH:9][CH:8]=[CH:7][CH:6]=4)[NH:3]3)[CH:19]=2)[CH2:28][CH2:27]1

参加物

5

反応物 3

HCID 24287Tin tetrachlorideHCID 308071ethyl 2-(1H-1,3-benzodiazol-2-yl)acetateHCID 219285192-Amino-5-(4-methyl-1-piperazinyl)benzonitrile

生成物 1

HCID 178480624HCID 178480624、化合物

試薬・触媒・溶媒 1

HCID 111,2-Dichloroethane溶媒

反応条件

温度
80 °C

実験手順

Ethyl 2-benzimidazol-2-ylacetate (1.1 eq) and 2-amino-5-(4-methylpiperazinyl)benzenecarbonitrile (1.0 eq) were dissolved in 1,2-dichloroethane, and then SnCl4 (11 eq) was added. The mixture was heated at reflux overnight. Upon cooling, the mixture was concentrated in vacuo. NaOH (3 M) was added to the solid, and the mixture heated at 80° C. for 0.5 hours. The solid was filtered and washed sequentially with H2O, CH2Cl2, and acetone. LC/MS indicated that the product was present in the acetone layer and the solid. These fractions were combined and purified by silica gel chromatography (5-10% MeOH in CH2Cl2 with 1% Et3N) to give the desired product. LC/MS m/z 375.4 (MH+), Rf 1.65 minutes.

後処理

  1. temperatureThe mixture was heated
  2. temperatureat reflux overnight
  3. temperatureUpon cooling
  4. concentrationthe mixture was concentrated in vacuo
  5. additionNaOH (3 M) was added to the solid
  6. filtrationThe solid was filtered
  7. washwashed sequentially with H2O, CH2Cl2, and acetone
  8. custompurified by silica gel chromatography (5-10% MeOH in CH2Cl2 with 1% Et3N)

出典と根拠

ORDレコード
ord-f2e1585b151d40ecb98e8ce46ec367ea
出典データセット
uspto-grants-2004_10
特許番号
US06800760B2

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