Hydrochloric Acid → HCID 21974247, compound

HRID 11474Notes

Reaction equation

HRID 11474 reaction equation
[ClH:1].C(OCC)(=O)C.[C:8]12([CH2:18][CH2:19][N:20]([CH2:33][CH2:34][CH2:35][CH2:36][CH3:37])[C:21]([NH:23][CH2:24][CH2:25][CH2:26][C:27]3[CH:32]=[CH:31][N:30]=[CH:29][CH:28]=3)=[O:22])[CH2:17][CH:12]3[CH2:13][CH:14]([CH2:16][CH:10]([CH2:11]3)[CH2:9]1)[CH2:15]2>C(Cl)(Cl)Cl>[ClH:1].[C:8]12([CH2:18][CH2:19][N:20]([CH2:33][CH2:34][CH2:35][CH2:36][CH3:37])[C:21]([NH:23][CH2:24][CH2:25][CH2:26][C:27]3[CH:28]=[CH:29][N:30]=[CH:31][CH:32]=3)=[O:22])[CH2:15][CH:14]3[CH2:16][CH:10]([CH2:11][CH:12]([CH2:13]3)[CH2:17]1)[CH2:9]2

Participants

5

Procedure

A 4 N solution of hydrogen chloride in ethyl acetate (0.400 ml, 1.60 mmol) was added to a solution of 1-[2-(1-adamantyl)ethyl]-1-pentyl-3-[3-(4-pyridyl)propyl]urea (Compound No. 1-1) (200 mg, 0.486 mmol) in chloroform (0.3 ml). The solvent was evaporated under reduced pressure, and the precipitated solid was washed with ethyl acetate and filtered off. The obtained crude crystals were recrystallized from 2-butanone (5.0 ml) to give 94 mg (43%) of the titled compound.

Workup

  1. customThe solvent was evaporated under reduced pressure
  2. washthe precipitated solid was washed with ethyl acetate
  3. filtrationfiltered off
  4. customThe obtained crude crystals
  5. customwere recrystallized from 2-butanone (5.0 ml)

Sources & evidence

ORD record
ord-7c9faa00da474823a42f76ed03b4aa2b
Source dataset
uspto-grants-2006_08
Patent number
US07098226B2

Reaction notes

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