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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1864656Generated: October 26, 2026

Iodine → HCID 11634929, compound

https://huagongshe.com/reaction/1864656

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantHCID 42626124HCID 42626124—
ReactantPhenyl 3-tert-butyl-1-(4-fluorophenyl)-1h-pyrazol-5-ylcarbamateHCID 46196891—
ProductHCID 11634929HCID 1163492935%

Reaction Steps

Method I2 was used with 7-(4-aminophenoxy)-1-methyl-1H-imidazo[4,5-b]pyridin-2(3H)-one (25 mg, 0.1 mmol) and phenyl 3-tert-butyl-1-(4-fluorophenyl)-1H-pyrazol-5-yl-carbamate (42 mg, 0.12 mmol) to afford the title compound (18 mg, 35%). 1H-NMR (δ, ppm, DMSO-d6): 1.29 (s, 9H, t-Bu), 3.46 (s, 3H, CH3N), 6.37 (s, 1H, HPyz,4), 6.41 (d, 1H, HPy,6), 7.13 (d, 2H, Harom,Ph,3+5), 7.38 (t, 2H, Harom,4-F-Ph,3+5), 7.48 (d, 2H, Harom,Ph,2+6), 7.57 (dd, 2H, Harom,4-F-Ph,2+6), 7.80 (d, 1H, HPy,6), 8.38 (s, 1H, NHurea), 9.08 (s, 1H, NHurea), 11.61 (bs, 1H, NHPy3). LC-MS (m/z): 516 (M+H, 100). Acc. mass (C27H26N7O3F): calculated 516.2159, found 516.2086.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07625922B2
Source datasetuspto-grants-2009_12
ORD IDord-3bafbeaa6288400597465930fb4c263b
Source noteuspto-grants-2009_12