Carbon Disulfide → HCID 178505424、化合物

HRID 1493321ノート

反応式

HRID 1493321 の反応式
[C:1](=[S:3])=S.[Cl:4][C:5]1[CH:10]=[CH:9][C:8]([CH2:11][NH:12][C:13]2[CH:19]=[CH:18][C:17]([F:20])=[CH:16][C:14]=2[NH2:15])=[CH:7][CH:6]=1>C(O)C>[Cl:4][C:5]1[CH:10]=[CH:9][C:8]([CH2:11][N:12]2[C:13]3[CH:19]=[CH:18][C:17]([F:20])=[CH:16][C:14]=3[N:15]=[C:1]2[SH:3])=[CH:7][CH:6]=1

参加物

4

反応物 2

HCID 6348Carbon DisulfideHCID 149529912-(4-Chlorobenzylamino)-5-fluoroaniline

生成物 1

HCID 178505424HCID 178505424、化合物

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

25 ml of carbon disulfide are added to 35.2 g of 2-(4-chlorophenylmethylamino)-5-fluoroaniline, prepared in Example 8, dissolved in 500 ml of ethanol. The mixture is refluxed for 12 hours and allowed to return to room temperature. After standing for a few hours, the crystals are filtered off and washed with ethanol and then with isopropanol and ether to give 33 g of 1-(4-chlorophenylmethyl)-2-mercapto-5-fluorobenzimidazole in the form of crystals melting at 215° C.

後処理

  1. customprepared in Example 8
  2. temperatureThe mixture is refluxed for 12 hours
  3. customto return to room temperature
  4. waitAfter standing for a few hours
  5. filtrationthe crystals are filtered off
  6. washwashed with ethanol

出典と根拠

ORDレコード
ord-8a68cad5b4c04bb7b845f2770ec0417d
出典データセット
uspto-grants-1991_06
特許番号
US05021443

反応ノート

読み込み中…