Isopropanol → Urea, (4-methoxyphenyl)-

HRID 1744796Notes

Reaction equation

HRID 1744796 reaction equation
C([N:5](CCCC)CCCC)CCC.[CH3:14][O:15][C:16]1[CH:21]=[CH:20][C:19]([N:22]=[C:23]=[O:24])=[CH:18][CH:17]=1.C(O)(C)C.C([O-])(=O)C.[NH4+]>O.CO.CN(C=O)C>[CH3:14][O:15][C:16]1[CH:17]=[CH:18][C:19]([NH:22][C:23]([NH2:5])=[O:24])=[CH:20][CH:21]=1

Participants

8

Reactant 4

HCID 3776IsopropanolHCID 7622Tributylamine2×HCID 794431-Isocyanato-4-methoxybenzeneHCID 517165Ammonium Acetate

Product 1

HCID 74066Urea, (4-methoxyphenyl)-Yield 55%

Reagents, catalysts & solvents 3

HCID 887MethanolSolvent2×HCID 962WaterSolventHCID 6228DimethylformamideSolvent

Procedure

P1-(cytidine 5′-)tetraphosphate, ditributylammonium salt (50 mg, 0.043 mmol: prepared from the tetraammonium salt by treatment with Dowex 50W×4 H+ in water, followed by mixing the protonated species with an excess of tributylamine in methanol, stripping and lyophilization) was dissolved in dry DMF (1 mL) and tributylamine (10 uL, 0.43 mmol), and p-methoxyphenylisocyanate 8.4 uL, 0.648 mmol) were added in a single portion. The homogeneous reaction mixture was heated overnight at 35° C., whereupon TLC (silica gel, 50% isopropanol/50% ammonium hydroxide) and HPLC (C18) indicated a substantial conversion to a single product. The solvent was removed on a rotary evaporator and the residue dissolved in water (1 mL). The product was isolated by repeated injections onto a semi-preparative HPLC column (Alltech Nucleotide/Nucleoside C18, 7 um, 10 X 250 mm, gradient from 0.1 M ammonium acetate to methanol over 30 minutes, 5 mL/min, monitor at 260 nm). Stripping and lyophilization gave the p-methoxyphenylurea (b 24 mg, 55% yield), as the tetraammonium salt.

Workup

  1. customThe solvent was removed on a rotary evaporator
  2. dissolutionthe residue dissolved in water (1 mL)
  3. customThe product was isolated

Sources & evidence

ORD record
ord-16852fe30fff4981ac20f1aad8b9d5d8
Source dataset
uspto-grants-2006_03
Patent number
US07018985B1

Reaction notes

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