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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522032Generated: October 30, 2026

[3-Fluoro-2-(trifluoromethyl)phenyl]boronic acid → HCID 86713922, compound

https://huagongshe.com/reaction/522032

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[3-Fluoro-2-(trifluoromethyl)phenyl]boronic acidHCID 17749939—
Reactanttert-butyl N-[2-bromo-4-[[5-[(2S,5R,6R)-5-(tert-butoxycarbonylamino)-6-fluoro-oxepan-2-yl]-1-methyl-pyrazol-4-yl]carbamoyl]thiazol-5-yl]carbamateHCID 86713830—
ProductHCID 86713922HCID 86713922—

Reaction Steps

Following the procedure for Example 101 starting from tert-butyl N-[2-bromo-4-[[5-[(2S,5R,6R)-5-(tert-butoxycarbonylamino)-6-fluoro-oxepan-2-yl]-1-methyl-pyrazol-4-yl]carbamoyl]thiazol-5-yl]carbamate (Intermediate 88), and replacing 3,6-dihydro-2H-pyran-4-boronic acid pinacol ester with (3-fluoro-2-(trifluoromethyl)phenyl)boronic acid gave 267. 1H NMR (400 MHz, DMSO-d6) δ 9.25 (s, 1H), 7.87-7.76 (m, 2H), 7.66-7.50 (m, 2H), 7.44 (s, 2H), 4.90 (dd, J=7.6, 3.8 Hz, 1H), 4.82-4.50 (m, 1H), 3.95-3.75 (m, 2H), 3.70 (s, 3H), 3.13 (dd, J=21.1, 8.4 Hz, 1H), 2.22-2.11 (m, 1H), 1.79-1.51 (m, 5H). LCMS (ES+) m/z 517 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09328106B2
Source datasetuspto-grants-2016_05
ORD IDord-65a7388a914a494e98a4bb33bd84b6fc
Source noteuspto-grants-2016_05