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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946977Generated: November 1, 2026

Acetic Acid → 3-(2-methylsulfanyl-pyrimidin-4-yl)-1H-indazole

https://huagongshe.com/reaction/1946977

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactanttert-Butyl carbazateHCID 70091—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant(2-Fluoro-phenyl)-(2-methylsulfanyl-pyrimidin-4-yl)-methanoneHCID 59743427—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product3-(2-methylsulfanyl-pyrimidin-4-yl)-1H-indazoleHCID 5974335163.7%

Reaction Steps

tert-Butylcarbazate (899 mg, 6.8 mmol) and acetic acid (0.5 mL) were added to a mixture of (2-fluoro-phenyl)-(2-methylsulfanyl-pyrimidin-4-yl)-methanone (840 mg, 3.4 mmol) in MeOH. The resulting mixture was heated at reflux for 16 h; it was then cooled to RT and partitioned between EtOAc and aqueous sodium bicarbonate. The organic layer was separated and dried over Na2SO4, filtered and evaporated under reduced pressure. The residue was placed in a sealed tube with DBU (0.79 mL, 5.3 mmol) and THF. The resulting mixture was heated to 150° C. in a microwave reactor for 30 minutes. The reaction mixture was then evaporated under reduced pressure and the crude residue was purified by flash chromatography (hexane/EtOAc, 4/1) to afford 525 mg of 3-(2-methylsulfanyl-pyrimidin-4-yl)-1H-indazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399462B2
Source datasetuspto-grants-2013_03
ORD IDord-996d2bc7868c4cff9db18c33dfecf9f4
Source noteuspto-grants-2013_03