Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1089247Generated: October 31, 2026

Triethylamine → HCID 13989893, compound

https://huagongshe.com/reaction/1089247

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantO-[3-(Benzyloxy)propyl]hydroxylamineHCID 13989887—
ReactantN-(4,6-dichloro-2-formamido-pyrimidin-5-yl)formamideHCID 13989892—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 13989893HCID 1398989350.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04965270
Source datasetuspto-grants-1990_10
ORD IDord-333967a71c8b4187958a03cca019a60e
Source noteuspto-grants-1990_10