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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2039674Generated: November 2, 2026

Sodium percarbonate → HCID 23634345, compound

https://huagongshe.com/reaction/2039674

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium percarbonateHCID 159762—
ReactantHCID 23634344HCID 23634344—
SolventPropan-2-one--water (1/1)HCID 18366337—
ProductHCID 23634345HCID 2363434543%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 1-(6-tert-butylpyrimidin-4-yl)-3-[4-(2-cyanopyridin-4-yloxy)-2-fluoro-phenyl]urea (141 mg, 0.35 mmol) and sodium percarbonate (with 25% H2O2) (218 mg, 1.4 mmol, 4.0 eq) in 2:1 v/v acetone/water (11 mL) was stirred at 60° C. for 16 h. The reaction was partitioned between ethyl acetate and water, and the aqueous layer was extracted with ethyl acetate (2×100 mL). The combined organic layers were washed with water and brine, dried over sodium sulfate, filtered, and evaporated under reduced pressure. Trituration from methanol afforded the title compound (63 mg, 43%) as a white solid. 1H-NMR (DMSO-d6) 10.32 (broad s, 1H), 10.08 (broad s, 1H), 8.75 (d, J=1.2 Hz, 1H), 8.51 (d, J=5.4 Hz, 1H), 8.23 (t, J=9.3 Hz, 1H), 8.12 (broad s, 1H), 7.71 (broad s, 1H), 7.61 (d, J=1.2 Hz, 1H), 7.40 (d, J=2.4 Hz, 1H), 7.36 (dd, J=11.4, 2.4 Hz, 1H), 7.18 (dd, J=5.7, 2.7 Hz, 1H), 7.08 (ddd, J=9.0, 2.7, 1.5 Hz, 1H), 1.26 (s, 9H); LC-MS m/z 425 [M+H]+, RT=3.16 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580798B2
Source datasetuspto-grants-2013_11
ORD IDord-2cb5edff17d748a3bfa85794b756f8f9
Source noteuspto-grants-2013_11