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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912547Generated: November 2, 2026

Triethylamine → HCID 57613446, compound

https://huagongshe.com/reaction/912547

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178503087HCID 178503087—
SolventAcetonitrileHCID 6342—
ProductHCID 57613446HCID 57613446—

Reaction Conditions

Temperature85 °C

Reaction Steps

POCl3 (1.51 mL, 16.2 mmol, 3.0 eq.) is added slowly to a suspension of 6-methylsulfanyl-[4,5′]bipyrimidinyl-4′-ol 6 (1.20 g, 5.44 mmol) and triethyl amine (0.76 mL, 5.44 mmol, 1.0 eq.) in acetonitrile (30 ml). After heating at 85° C. for 2 hours, the reaction mixture is cooled to room temperature, poured into ice-water, neutralized by saturated NaHCO3 solution, and then extracted with ethyl acetate. The organic layer is washed with brine and dried over Na2SO4, filtered and concentrated. The crude product is purified by silica gel flash chromatography eluting with ethyl acetate in hexanes from 0% to 40% to give 4′-chloro-6-methylsulfanyl-[4,5′]bipyrimidinyl as a white solid. 1H NMR 400 MHz (DMSO-d6) δ 9.19 (s, 1H), 9.12 (d, 1H, J=1.2 Hz), 9.07 (s, 1H), 7.91 (d, 1H, J=1.6 Hz), 2.62 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08026243B2
Source datasetuspto-grants-2011_09
ORD IDord-3dfdc154fb9c40c496c2749cd1f4cb4d
Source noteuspto-grants-2011_09