HCID 178466943, compound → HCID 178433290, compound

HRID 745765Notes

Reaction equation

HRID 745765 reaction equation
[CH3:1][C:2]1[N:3]=[CH:4][NH:5][C:6]=1[CH2:7][S:8][CH2:9][CH2:10][NH:11][C:12]1[CH:21]=[C:20]([O:22]CC)[C:19]2[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=2)[N:13]=1>Cl>[CH3:1][C:2]1[N:3]=[CH:4][NH:5][C:6]=1[CH2:7][S:8][CH2:9][CH2:10][NH:11][C:12]1[CH2:21][C:20](=[O:22])[C:19]2[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=2)[N:13]=1

Participants

3

Procedure

(Found: C, 63.2; H, 6.5; N, 16.1; S, 9.1. C18H22N4CS requires: C, 63.1; H, 6.5; N, 16.4; S, 9.4.) 2-[2-(4-Methyl-5-imidazolylmethylthio)ethylamino]-4-ethoxyquinoline (1.69 gms) and concentrated HCl (30 mls) were refluxed together for 17 hours. The solution was evaporated to dryness, the residue dissolved in water and basified with potassium carbonate. The precipitated oil was separated by decantation, washed with water and crystallised from isopropanol-water to give 2[-2-(4-methyl-5-imidazolylmethylthio)ethylamino]-4-quinolone.

Workup

  1. customThe solution was evaporated to dryness
  2. dissolutionthe residue dissolved in water and basified with potassium carbonate
  3. customThe precipitated oil was separated by decantation
  4. washwashed with water
  5. customcrystallised from isopropanol-water

Sources & evidence

ORD record
ord-6a3421dee58d47c585b0278f9690989c
Source dataset
uspto-grants-1986_07
Patent number
US04600720

Reaction notes

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