Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 15681692 | HCID 15681692 | — |
| Product | HCID 45262917 | HCID 45262917 | 7% |
Reaction Steps
5-Hydroxy-1,4,5,6-tetrahydropyrimidine (JOC, 1966, 31, 3838; 1 g, 10 mmol) was dissolved in glacial acetic acid (25 ml) with stirring, and thionylchloride (0.73 ml, 10 mmol) was added dropwise. The resulting solution was refluxed 19 hours, then evaporated to dryness in vacuo. The residue was taken up in water (5 ml), the pH adjusted to 12 (sat. Na2CO3), and extracted with chloroform. The chloroform was dried (MgSO4) and evaporated in vacuo to 440 mg (25%) product as a clear oil identified by 400 MHz nmr. The oil was converted to its HCl salt in anhydrous ethanol with addition of IM HCl in ether. After evaporation of solvents the resulting crude HCl salt was recrystallized from ethanol to yield 128 mg (7%) white crystals, mp 287°-289° C. 400 MHz nmr and ir confirmed product. Calculated: C 40.34, H 6.2, N 15.69; found: C 40.45, H 6.19, N 15.53.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05403845 |
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| Source dataset | uspto-grants-1995_04 |
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| ORD ID | ord-38958a1d739e4abfafa20241effc55d6 |
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| Source note | uspto-grants-1995_04 |
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