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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1993523Generated: October 30, 2026

trans-2-Phenylcyclopropyl isocyanate → (+/-)-trans-N-(4-(4-Ethylaminopyrimidin-6-yl-oxy)-phenyl)-N'-(2-phenyl-cyclopropyl)-urea

https://huagongshe.com/reaction/1993523

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttrans-2-Phenylcyclopropyl isocyanateHCID 255285—
Reactant4-(4-Ethylaminopyrimidin-6-yloxy)anilineHCID 58659385—
SolventTetrahydrofuranHCID 8028—
Product(+/-)-trans-N-(4-(4-Ethylaminopyrimidin-6-yl-oxy)-phenyl)-N'-(2-phenyl-cyclopropyl)-ureaHCID 68535936—

Reaction Steps

To a solution of 4-(4-ethylaminopyrimidin-6-yl-oxy)-aniline (Stage 89.1; 271 mg, 1.177 mmol) In THF (5 ml) under N2-atmosphere, trans-2-phenyl-cyclopropyl-isocyanate (188 mg, 1.18 mmol; Aldrich) Is added. Then the solution is stirred for 8 h, whereas a precipitate is formed. Filtration and washing with THF and ether yields the title compound: m.p.: 205-206° C.; 1H-NMR (DMSO-d6): 8.50 (s, HN), 8.11 (s, 1H), 7.42 (d, 2H), 7.27 (m, 3H), 7.15 (m, 3H), 7.01 (d, 2H), 6.67 (s, HN), 5.67 (s, 1H), 3.25 (m, 2H), 2.74 (m, 1H), 1.98 (m, 1H), 1.17 (m, 2H), 1.09 (t, 3H); Anal.: CHN.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652022B2
Source datasetuspto-grants-2010_01
ORD IDord-05d935c7ef5f4efd863c57dd4a730c3b
Source noteuspto-grants-2010_01