Hydrochloric Acid → HCID 54236563, compound

HRID 413202Notes

Reaction equation

HRID 413202 reaction equation
[NH2:1][NH:2][C:3]([NH2:5])=[S:4].[CH:6]1([NH:12][C:13](=[O:24])[CH2:14][CH2:15][C:16](=O)[C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[CH2:11][CH2:10][CH2:9][CH2:8][CH2:7]1.Cl.O>CO>[NH2:5][C:3]([NH:2][N:1]=[C:16]([C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)[CH2:15][CH2:14][C:13]([NH:12][CH:6]1[CH2:11][CH2:10][CH2:9][CH2:8][CH2:7]1)=[O:24])=[S:4]

Participants

6

Procedure

Thiosemicarbazide (1.75 g, 19.2 mmol) was added to a solution of N-cyclohexyl-4-oxo-4-phenyl-butyramide (3.30 g, 11.7 mmol), prepared in the previous step, in 40 ml of methanol plus 3.2 ml of 1 N HCl plus 3.2 ml of water and the reaction stirred at room temperature for 21 hours. The solid formed was removed by filtration and dried to give 2.69 g of a white solid. The filtrate was concentrated under reduced pressure to remove the methanol. The residue was partitioned between methylene chloride and water. The organic layer was separated, wash ed multiple times with water, dried (MgSO4) and the solvent removed under reduced pressure to give 1.10 g of a white foam. The initial solid filtered from the reaction was dissolved in methylene chloride, washed multiple times with water, dried (MgSO4) and the solvent removed under reduced pressure to give a white foam. Both materials were combined and crystallized from methylene chloride-ethyl acetate to give the title compound (3.31 g, 69%) as a white solid, mp 89-92° C.

Workup

  1. customThe solid formed
  2. customwas removed by filtration
  3. customdried

Sources & evidence

ORD record
ord-07aab5ed06884bce8a625433d8694f71
Source dataset
uspto-grants-2003_05
Patent number
US06566375B1

Reaction notes

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