HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1463268Generated: November 2, 2026
Phosphorus oxychloride → HCID 18982115, compound
https://huagongshe.com/reaction/1463268
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 178490296 | HCID 178490296 | — |
| Product | HCID 18982115 | HCID 18982115 | 83.2% |
Reaction Steps
A mixture of 4,6-dihydroxy-5-(2-furanylcarbonyl)amino-2-[(4-methoxyphenyl)ethyl]aminopyrimidine (408 mg) and phosphorus oxychloride (5 ml) was heated at 90° C. for 3 hours. The excess phosphorus oxychloride was removed by evaporation, in vacuo, and then by azeotroping with toluene (2×50 ml). The residue was added to water and the resultant precipitate filtered off, washed with water and dried. There was thus produced 7-chloro-2-(2-furyl)-5-[2-(4-methoxyphenyl)ethyl]amino oxazolo[5,4-d]pyrimidine (340 mg, 83.2% yield); m.p. 169.5°-171° C.: NMR:DMSO-d6 : 2.80(t, 2H, ArCH2), 3.48(q, 2H, CH2NH), 3.72(s, 3H, OMe), 6.80(m, 1H, furyl-H), 6.85(d, 2H, ArH), 7.16(d, 2H, ArH), 7.44(d, 1H, furyl-H), 8.07(m, 1H, furyl-H), 8.13(brs, 1H, NH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05300509 |
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| Source dataset | uspto-grants-1994_04 |
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| ORD ID | ord-895bb94d256a4c988d489b973216ad70 |
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| Source note | uspto-grants-1994_04 |
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