Hydrochloric Acid → HCID 23037305, compound

HRID 1709541Notes

Reaction equation

HRID 1709541 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[N:16]([CH2:17][C:18]([NH:20][CH2:21][CH2:22][CH2:23][N:24]([CH2:27][CH3:28])[CH2:25][CH3:26])=[O:19])[C:11]3=[N:12][CH:13]=[CH:14][CH:15]=[C:10]3[N:9]=2)=[CH:4][CH:3]=1.Cl>C(O)(C)C>[ClH:1].[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[N:16]([CH2:17][C:18]([NH:20][CH2:21][CH2:22][CH2:23][N:24]([CH2:25][CH3:26])[CH2:27][CH3:28])=[O:19])[C:11]3=[N:12][CH:13]=[CH:14][CH:15]=[C:10]3[N:9]=2)=[CH:4][CH:3]=1

Participants

4

Procedure

Approximately 5.7 g of crude 2-(4-chlorophenyl)-N-[3-(diethylamino)propyl]-3H-imidazo[4,5-b]pyridine-3-acetamide was dissolved in hot isopropyl alcohol and acidified with ethereal hydrogen chloride. The solvents were removed under reduced pressure. The residue was redissolved in hot isopropyl alcohol and cooled to room temperature while a solid formed. The solid was collected by filtration, rinsed with an isopropyl alcohol-isopropyl ether solution and finally rinsed with isopropyl ether. Drying under high vacuum gave a white solid weighing 5.0 g, mp 173°-177° C.

Workup

  1. customThe solvents were removed under reduced pressure
  2. dissolutionThe residue was redissolved in hot isopropyl alcohol
  3. customformed
  4. filtrationThe solid was collected by filtration
  5. washrinsed with an isopropyl alcohol-isopropyl ether solution
  6. washfinally rinsed with isopropyl ether
  7. customDrying under high vacuum
  8. customgave a white solid

Sources & evidence

ORD record
ord-0e15c68baac140e08a922d00c2471480
Source dataset
uspto-grants-1990_08
Patent number
US04948800

Reaction notes

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