Thiourea → Methyl 5-(2-aminothiazol-4-yl)valerate

HRID 1902559Notes

Reaction equation

HRID 1902559 reaction equation
[NH2:1][C:2]([NH2:4])=[S:3].Cl[CH2:6][C:7](=O)[CH2:8][CH2:9][CH2:10][CH2:11][C:12]([O:14][CH3:15])=[O:13]>C(O)C>[NH2:1][C:2]1[S:3][CH:6]=[C:7]([CH2:8][CH2:9][CH2:10][CH2:11][C:12]([O:14][CH3:15])=[O:13])[N:4]=1

Participants

4

Conditions

Temperature
20 °C

Procedure

Thiourea (15.7 g) and methyl 7-chloro-6-oxoheptanoate (39.7 g) are mixed in ethanol (200 cc). The mixture is stirred for 20 hours at a temperature of about 20° C.; gradual dissolution of the reactants is observed. The solution is concentrated to dryness under reduced pressure (25 mm Hg; 3.3 kPa) at 40° C. The residue is stirred in a mixture of methylene chloride (250 cc) and N sodium hydroxide solution (250 cc). The insoluble product is filtered off, washed with water and recrystallised by dissolving it in boiling water (350 cc) and cooling to 5° C. The resulting crystals are washed with water (3×30 cc), ethanol (3×30 cc) and diethyl ether (2×50 cc) and dried at 20° C. under reduced pressure (0.1 mm Hg; 0.013 kPa) to yield methyl 5-(2-aminothiazol-4-yl)valerate (31 g), as a white solid, m.p.=131° C.

Workup

  1. dissolutiongradual dissolution of the reactants
  2. concentrationThe solution is concentrated to dryness under reduced pressure (25 mm Hg; 3.3 kPa) at 40° C
  3. stirringThe residue is stirred in a mixture of methylene chloride (250 cc) and N sodium hydroxide solution (250 cc)
  4. filtrationThe insoluble product is filtered off
  5. washwashed with water
  6. customrecrystallised
  7. dissolutionby dissolving it
  8. temperaturecooling to 5° C
  9. washThe resulting crystals are washed with water (3×30 cc), ethanol (3×30 cc) and diethyl ether (2×50 cc)
  10. customdried at 20° C. under reduced pressure (0.1 mm Hg; 0.013 kPa)

Sources & evidence

ORD record
ord-7da61c55bb01422cb73892c494c0e771
Source dataset
uspto-grants-1982_12
Patent number
US04363909

Reaction notes

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