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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 630465Generated: October 30, 2026

5-Bromo-2-chloropyrimidine → Methyl 1-(5-bromopyrimidin-2-yl)-3-(methylthio)-1H-indole-6-carboxylate

https://huagongshe.com/reaction/630465

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-2-chloropyrimidineHCID 606665—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantMethyl 3-(methylthio)-1H-indole-6-carboxylateHCID 118666085—
SolventDimethylformamideHCID 6228—
ProductMethyl 1-(5-bromopyrimidin-2-yl)-3-(methylthio)-1H-indole-6-carboxylateHCID 118666039—

Reaction Conditions

Temperature120 °C

Reaction Steps

Potassium tert-butylate (4.41 g, 39.36 mmol) and 5-bromo-2-chloro-pyrimidine (5.0 g, 26.2 mmol) were added to a solution of methyl 3-(methylthio)-1H-indole-6-carboxylate (5.8 g, 26.2 mmol) in DMF (60 mL). The resulting mixture was heated at 120° C. for 16 h, then cooled and poured onto ice-cold water (100 mL). The mixture was extracted with MTBE (3×50 mL) and the combined organic layers were dried over sodium sulfate and evaporated. The crude material was purified by column chromatography [100-200 mesh silica; ethyl acetate/hexane=1:9]. White solid. Yield: 6.0 g (61% of theory). HPLC-MS (method 5): Rt=4.15 min; m/z [M+H]+=379

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315490B2
Source datasetuspto-grants-2016_04
ORD IDord-c8341893b4f244fdb52e28f0aba4469e
Source noteuspto-grants-2016_04