Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 85480Generated: October 25, 2026

Isopropyl iodide → Methyl 6-bromo-3-formyl-1-isopropyl-1H-indazole-4-carboxylate

https://huagongshe.com/reaction/85480

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropyl iodideHCID 6362—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 178497028HCID 178497028—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductMethyl 6-bromo-3-formyl-1-isopropyl-1H-indazole-4-carboxylateHCID 71742648—

Reaction Steps

To a stirred solution of methyl 6-bromo-3-formyl-1H-indazole-4-carboxylate 1 (11.5 g, 40.63 mmol) in DMF (230 mL)) was added K2CO3 (14.08 g, 102.02 mmol) at RT under argon, and stirred for 10 min. Then 2-iodopropane (7.24 g, 42.58 mmol) was added at RT and the mixture stirred at 40° C. for 2 h. The reaction mixture was diluted with cold water and extracted with ethyl acetate (4×300 mL). The combined organic layers were washed with water, brine, dried over anhydrous Na2SO4, filtered, and concentrated. The crude residue (12.4 g) was purified by silica gel chromatography (eluent: 0-10% ethyl acetate: pet ether) to afford the title compound as an off white solid (5.55 g, 42%). 1H NMR (CDCl3, 400 MHz): δ 1.659 (d, J=6.4 Hz, 6H), 4.017 (s, 3H), 4.862-4.960 (m, 1H), 7.807 (s, 1H), 7.854 (s, 1H), 10.375 (s, 1H). HPLC: 98.66%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846935B2
Source datasetuspto-grants-2014_09
ORD IDord-bed8b3597309468483d1553451c55f1c
Source noteuspto-grants-2014_09