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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2404036Generated: October 30, 2026

Acetic Acid → HCID 86713577, compound

https://huagongshe.com/reaction/2404036

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant3,5-DimethoxyanilineHCID 66301—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant4-(Methylamino)-2-(methylthio)pyrimidine-5-carbaldehydeHCID 10607520—
SolventMethanolHCID 887—
ProductHCID 86713577HCID 86713577—

Reaction Steps

A mixture of 4-(methylamino)-2-(methylthio)pyrimidine-5-carbaldehyde (1.0 g, 5.46 mmol) and 3,5-dimethoxyaniline (840 mg, 5.46 mmol) in methanol (60 mL) was stirred at RT for 3 h, followed by the addition of sodium cyanoborohydride (520 mg, 8.20 mmol) and 1 mL of acetic acid. The reaction mixture was then stirred at RT for another 4 h. LCMS showed the reaction was completed. The reaction was quenched by 30 mL of 1N HCl, then stirred for 0.5 h and extracted with ethyl acetate (3×50 mL). The organic layers were separated, combined, washed with saturated aqueous solution of sodium bicarbonate and brine, dried over sodium sulfate, filtered and concentrated to afford the title compound (crude 1.2 g, 69%) as a white solid, which was directly used in the next step without further purification. MS (ES+) C15H20N4O2S requires: 320. found: 321 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802697B2
Source datasetuspto-grants-2014_08
ORD IDord-b613e3dd3b7341df9a9d93fda8642a10
Source noteuspto-grants-2014_08