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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1463266Generated: November 1, 2026

Ammonia → HCID 9884818, compound

https://huagongshe.com/reaction/1463266

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantWaterHCID 962—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 18982115HCID 18982115—
SolventEthanolHCID 702—
ProductHCID 9884818HCID 988481848.6%

Reaction Conditions

Temperature100 °C

Reaction Steps

7-chloro-2-(2-furyl)-5-[2-(4-methoxyphenyl)ethyl]amino-oxazolo[5,4-d]pyrimidine (0.5 g) and ammonium chloride (0.1 g) were added to a saturated solution of ammonia in ethanol (20 ml) and sealed in a Caries tube. The sealed tube was then heated at 100° C. for 18 hours. The cooled reaction mixture was poured into water (200 ml) and the resultant precipitate removed by filtration. The solid was recrystallised from methanol to afford 7-amino-2-(2-furyl)-5-[2-(4-methoxyphenyl)ethyl]amino-oxazolo[5,4-d]pyrimidine (0.23 g, 48.6%), m.p. 194°-196° C.; microanalysis, found: C, 61.5; H, 4.8; N, 19.5%; C18H17N5O3 requires: C, 61.5; H, 4.9; N, 19.9%; NMR (DMSO-d6); 2.76(t,2H ArCH2), 3.44(brq 2H, CH2NH), 3.72(s, 3H, OMe), 6.70(m, 1 H furyl-H), 6.28(brs, 1H NH), 6.84(d, 2H, ArH), 7.13(complex, 5H ArH, NH2 furyl-H), 7.89(m, 1H, furyl-H); m/e [M+H]+ 352.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05300509
Source datasetuspto-grants-1994_04
ORD IDord-3e7f895a1248418eac9c51eee304611d
Source noteuspto-grants-1994_04