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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1173431Generated: November 1, 2026

2-Iodo-1,3-oxazole → 4-[(2-{[4-(1,3-Oxazol-2-yl)phenyl]oxy}ethyl)(2,2,2-trifluoroethyl)amino]-2-(trifluoromethyl)benzonitrile

https://huagongshe.com/reaction/1173431

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Iodo-1,3-oxazoleHCID 18359209—
Reactant4-[(2-{[4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]oxy}ethyl)(2,2,2-trifluoroethyl)amino]-2-(trifluoromethyl)benzonitrileHCID 86623735—
CatalystHCID 178418397HCID 178418397—
Product4-[(2-{[4-(1,3-Oxazol-2-yl)phenyl]oxy}ethyl)(2,2,2-trifluoroethyl)amino]-2-(trifluoromethyl)benzonitrileHCID 11698189—

Reaction Steps

Synthesized as described in Example 40B from 4-[(2-{[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]oxy}ethyl)(2,2,2-trifluoroethyl)amino]-2-(trifluoromethyl)benzonitrile (Example 40A) and 2-iodo-1,3-oxazole (step A above), with the following exceptions: additional 2-iodo-1,3-oxazole (0.3 equiv) was added after 2 h of heating, additional Pd(PPh3)4 (0.005 g) was added after 4 h of heating, and heating was maintained for only 6 h: MS (ESI) m/z 456 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834063B2
Source datasetuspto-grants-2010_11
ORD IDord-9d9d6438dec44a2aab98dbe0918cc714
Source noteuspto-grants-2010_11