Carbon Disulfide → HCID 178527773, compound

HRID 2050315Notes

Reaction equation

HRID 2050315 reaction equation
Cl.[NH2:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[NH:9][CH2:10][CH2:11][CH2:12][N:13]1[CH2:18][CH2:17][N:16]([CH:19]([C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)[C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[CH2:15][CH2:14]1.[C:32](=S)=[S:33].C(=O)([O-])[O-].[Na+].[Na+]>C(O)C>[C:20]1([CH:19]([C:26]2[CH:27]=[CH:28][CH:29]=[CH:30][CH:31]=2)[N:16]2[CH2:15][CH2:14][N:13]([CH2:12][CH2:11][CH2:10][N:9]3[C:4]4[CH:5]=[CH:6][CH:7]=[CH:8][C:3]=4[N:2]=[C:32]3[SH:33])[CH2:18][CH2:17]2)[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=1

Participants

5

Procedure

A mixture of 4.37 parts of N-(2-aminophenyl)-4-(diphenylmethyl)-1-piperazinepropanamine hydrochloride, 38 parts of carbon disulfide, 2 parts of sodium carbonate and 40 parts of ethanol is stirred and refluxed for 20 hours. The reaction mixture is evaporated and water is added to the residue. The precipitated product is filtered off, washed with water and dissolved in trichloromethane. The solution is dried, filtered and evaporated. The residue is crystallized from 4-methyl-2-pentanone, yielding 1-{3-[4-(diphenylmethyl)-1-piperazinyl]propyl}-1H-benzimidazole-2-thiol; mp. 181.8° C.

Workup

  1. temperaturerefluxed for 20 hours
  2. customThe reaction mixture is evaporated
  3. additionwater is added to the residue
  4. filtrationThe precipitated product is filtered off
  5. washwashed with water
  6. dissolutiondissolved in trichloromethane
  7. customThe solution is dried
  8. filtrationfiltered
  9. customevaporated
  10. customThe residue is crystallized from 4-methyl-2-pentanone

Sources & evidence

ORD record
ord-b611306933d042cbb64084a847d789fc
Source dataset
uspto-grants-1980_04
Patent number
US04200641

Reaction notes

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