HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 13989893, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | O-[3-(Benzyloxy)propyl]hydroxylamine | HCID 13989887 | — |
| Reactant | N-(4,6-dichloro-2-formamido-pyrimidin-5-yl)formamide | HCID 13989892 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 13989893 | HCID 13989893 | 50.1% |
Reaction Steps
A mixture of 4,6-dichloro-2,5-diformamidopyrimidine (5.4 g, 23.0 mmol), 3-benzyloxyprop-1-oxyamine (4.14, 23.0 mmol), triethylamine (10 ml) and dioxan (50 ml) was stirred at reflux temperature for 3 hours, cooled, filtered and evaporated to dryness. Column chromatography on silica gel (eluted with chloroform-ethanol, 25:1) gave the title compound (4.38 g, 50%). IR: υmax (KBr) 3248, 1692, 1589, 1570, 1473, 1420 cm-1. 1H NMR: δH [(CD3)2SO] 1.88 (2H, quintet, J=6.3 Hz, CH2CH2CH2) 3.57 (2H, t, J=6.3 Hz, CH2OCH2Ph), 3.95 (2H, t, 6.3 Hz, CH2ONH), 4.47 (2H, s, CH2Ph), 7.32 (5H, m, Ph), 8.14 (1H, s, CHONH), 9.26 (1H, s, CHONH), 9.42 (1H, br.s, D2O exchangeable, NHOCH2), 10.83 (2H, br.s, 2×NHCHO).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04965270 |
| Source dataset | uspto-grants-1990_10 |
| ORD ID | ord-333967a71c8b4187958a03cca019a60e |
| Source note | uspto-grants-1990_10 |