Cyanoacetic acid → 6-Amino-1,3-bis(cyclohexylmethyl)uracil

HRID 1835002Notes

Reaction equation

HRID 1835002 reaction equation
[C:1]([CH2:3][C:4](O)=[O:5])#[N:2].[CH:7]1([CH2:13][NH:14][C:15]([NH:17][CH2:18][CH:19]2[CH2:24][CH2:23][CH2:22][CH2:21][CH2:20]2)=[O:16])[CH2:12][CH2:11][CH2:10][CH2:9][CH2:8]1>C(OC(=O)C)(=O)C>[NH2:2][C:1]1[N:14]([CH2:13][CH:7]2[CH2:8][CH2:9][CH2:10][CH2:11][CH2:12]2)[C:15](=[O:16])[N:17]([CH2:18][CH:19]2[CH2:24][CH2:23][CH2:22][CH2:21][CH2:20]2)[C:4](=[O:5])[CH:3]=1

Participants

4

Reactant 2

HCID 9740Cyanoacetic acidHCID 2315151,3-Bis(cyclohexylmethyl)urea

Product 1

HCID 222449716-Amino-1,3-bis(cyclohexylmethyl)uracilYield 94.2%

Reagents, catalysts & solvents 1

HCID 7918Acetic AnhydrideSolvent

Conditions

Temperature
80 °C

Procedure

Cyanoacetic acid (Aldrich, 21.0 g) was dissolved in acetic anhydride (260 ml). This solution was added to 1,3-bis(cyclohexylmethyl)urea (from step (a), 54.5 g) and the solution maintained at 80° C. for 2 h under nitrogen. Volatiles were removed in vacuo and the residual oil dried by evaporation of portions of 10% water-ethanol (3×400 ml). The residual solids were dissolved in ethanol (600 ml)-water (300 ml) at 80° C. with adjustment of the pH to 10 by addition of 10% aqueous sodium carbonate. The hot solution was diluted with water (75 ml) and cooled to ambient temperature. The colorless crystals which formed were filtered off, washed with water and dried at 0.5 Torr to give 6-amino-1,3-bis(cyclohexylmethyl)uracil (64.98 g, 94%), m.p. 138-141° C.; 1H-NMR (DMSO-d6) δ: 6.73 (br s, 2, NH2), 4.63 (s, 1, H-5), 3.67 (d, J=7.3 Hz, 2, NCH2), 3.57 (d, J=7.3 Hz, 2, NCH2), 1.55 and 1.09 (both m, 22, 2 cyclohexyl).

Workup

  1. customVolatiles were removed in vacuo
  2. dry with materialthe residual oil dried by evaporation of portions of 10% water-ethanol (3×400 ml)
  3. dissolutionThe residual solids were dissolved in ethanol (600 ml)-water (300 ml) at 80° C. with adjustment of the pH to 10
  4. additionby addition of 10% aqueous sodium carbonate
  5. additionThe hot solution was diluted with water (75 ml)
  6. temperaturecooled to ambient temperature
  7. customThe colorless crystals which formed
  8. filtrationwere filtered off
  9. washwashed with water
  10. customdried at 0.5 Torr

Sources & evidence

ORD record
ord-b506bd596dc94422b4cf26c91746084c
Source dataset
uspto-grants-2004_08
Patent number
US06770267B2

Reaction notes

Loading…