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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1424418Generated: November 1, 2026

Potassium Iodide → HCID 178470279, compound

https://huagongshe.com/reaction/1424418

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantDiisopropylethylamineHCID 81531—
ReactantEthyl 4-chloro-7-iodoquinazoline-2-carboxylateHCID 86649053—
ReactantHCID 178418806HCID 178418806—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 178470279HCID 17847027984%

Reaction Steps

To a solution of ethyl 4-chloro-7-iodoquinazoline-2-carboxylate (0.138 g, 0.38 mmol) in DMF (2 mL) at rt under argon were added potassium iodide (0.069 g, 0.42 mmol), DIEA (0.079 mL, 0.45 mmol), and 1H-pyrazol-3-amine (0.038 g, 0.46 mmol). The mixture was stirred at rt overnight then diluted with H2O (15 mL). The precipitate was collected by filtration, washed with H2O, and dried under high vacuum for several hours to afford ethyl 4-(1H-pyrazol-3-ylamino)-7-iodoquinazoline-2-carboxylate as a yellow solid (0.130 g, 84%). 1H NMR (300 MHz, DMSO-d6) δ1.34 (t, 3H), 4.38 (q, 2H), 7.14 (m, 1H), 7.72 (m, 1H), 7.94 (d, 1H), 8.28 (d, 1H), 8.48 (d, 1H), 10.92 (s, 1H), 12.58 (s, 1H); LC-MS (ESI) m/z 410 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927711B2
Source datasetuspto-grants-2015_01
ORD IDord-520970a5fa6747b7baf6f3b678b1ea46
Source noteuspto-grants-2015_01