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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1255205Generated: October 31, 2026

Iodine → Ethyl 1-[4-iodo-6-(2-methoxy-5-methylphenyl)pyridin-2-yl]-5-(trifluoromethyl)-1H-pyrazole-4-carboxylate

https://huagongshe.com/reaction/1255205

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantTert-Butyl nitriteHCID 10906—
ReactantEthyl 1-[4-amino-6-(2-methoxy-5-methylphenyl)pyridin-2-yl]-5-(trifluoromethyl)-1H-pyrazole-4-carboxylateHCID 67159525—
SolventChloroformHCID 6212—
ProductEthyl 1-[4-iodo-6-(2-methoxy-5-methylphenyl)pyridin-2-yl]-5-(trifluoromethyl)-1H-pyrazole-4-carboxylateHCID 67158744—

Reaction Conditions

Temperature60 °C

Reaction Steps

Tert-butyl nitrite (0.68 mL, 0.59 mmol) was added to a solution of the title compound from Example 19 Step E (1.2 g, 2.9 mmol) and iodine (0.87 g, 3.4 mmol) in chloroform (20 mL). The resulting mixture was heated at 60° C. for 30 min, cooled and quenched with aqueous sodium sulfite. Extraction with hexane-EtOAc, followed by silica gel flash chromatography using Hexane-EtOAc (20/1 to 7/1) provided the title compound: LCMS m/z 532.6 [M+H]+; 1H NMR (500 MHz, CDCl3) δ 8.54 (d, J=1.1 Hz, 1H), 8.15 (s, 1H), 7.98 (d, J=1.1 Hz, 1H), 7.79 (d, J=2.1 Hz, 1H), 7.25 (dd, J=8.5 Hz, 2.1 Hz, 1H), 6.94 (d, J=8.5 Hz, 1H), 4.43 (q, J=7.1 Hz, 2H), 3.93 (s, 3H), 2.39 (s, 3H), 1.42 (t, J=7.1 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455638B2
Source datasetuspto-grants-2013_06
ORD IDord-64aab6e373af4964ab1c63646a1f1ea1
Source noteuspto-grants-2013_06