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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 394784Generated: October 25, 2026

Sodium Carbonate → 2-[Bis(tert-butoxycarbonyl)amino]-5-(2'-methylthiophenyl)pyrimidine

https://huagongshe.com/reaction/394784

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2-(Methylthio)benzeneboronic acidHCID 2773543—
Reactanttert-butyl N-(5-bromopyrimidin-2-yl)-N-((tert-butoxy)carbonyl)carbamateHCID 11977091—
CatalystTetrabutylammonium BromideHCID 74236—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventBenzeneHCID 241—
Product2-[Bis(tert-butoxycarbonyl)amino]-5-(2'-methylthiophenyl)pyrimidineHCID 1817732096.3%

Reaction Steps

2-[Bis(tert-butoxycarbonyl)amino]-5-bromopyrimidine (2.00 g, 5.3 mmol) was dissolved in benzene (130 mL). 2-methylthiophenylboronic acid (2.24 g, 13.3 mmol), aq. sodium carbonate (13 mL, 2.0 M, 26 mmol), tetrabutyl ammonium bromide (86 mg, 0.26 mmol), and bis(triphenylphosphine)palladium(II)chloride (190 mg, 0.27 mmol) were added, and the resulting mixture was first purged with vacuum and argon, then refluxed 17 hours. The cooled mixture was diluted with EtOAc and water. The layers were separated, and the organic was dried over Na2SO4, filtered, and evaporated. The crude product was chromatographed on silica gel (50% EtOAc/hexanes), evaporated, and chromatographed a second time on silica gel (30-50% EtOAc/hexanes) to yield the desired product (2.13 g, 96%). 1H NMR (CDCl3): δ 8.81 (s, 2H), 7.41 (m, 2H), 7.25 (m, 2H), 2.39 (s, 3H), 1.49 (s, 18H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06602895B2
Source datasetuspto-grants-2003_08
ORD IDord-199091ef605e418ab7f06aa043e60a83
Source noteuspto-grants-2003_08