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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1519161Generated: November 3, 2026

4-(Bromomethyl)phenylacetic acid → HCID 77844320, compound

https://huagongshe.com/reaction/1519161

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Bromomethyl)phenylacetic acidHCID 4519056—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 90310688HCID 90310688—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 77844320HCID 7784432010.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of 6-cyclobutyl-3-(3,4-dihydro-2H-pyrido[3,2-b][1,4]oxazin-7-yl)-2-fluorophenol (50 mg, 0.17 mmol) and 2-(4-(bromomethyl)phenyl)acetic acid (38 mg, 0.17 mmol) in DMSO (1 mL) was treated with potassium tert-butoxide (38 mg, 0.33 mmol) and stirred for 16 hours at 80° Celsius. The reaction was then cooled to rt, filtered, and the filtrate subjected directly to HPLC purification to give (4-{[6-cyclobutyl-3-(3,4-dihydro-2H-pyrido[3,2-b][1,4]oxazin-7-yl)-2-fluorophenoxy]methyl}phenyl)acetic acid (8 mg, 9%). MS (ESI): mass calcd. for C26H25FN2O4, 448.18; m/z found, 449.2 [M+H]+. 1H NMR (600 MHz, CD3OD) δ 7.72 (s, 1H), 7.60 (s, 1H), 7.40 (d, J=8.1, 2H), 7.31 (d, J=8.1, 2H), 7.19 (d, J=6.0, 2H), 5.04 (s, 2H), 4.38-4.32 (m, 2H), 3.78-3.72 (m, 1H), 3.71-3.67 (m, 2H), 3.63 (s, 2H), 2.29-2.22 (m, 2H), 2.16-2.07 (m, 2H), 2.04-1.97 (m, 1H), 1.84 (t, J=9.6, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073876B2
Source datasetuspto-grants-2015_07
ORD IDord-3ce1549ca06d4f58b4354470a7ce1915
Source noteuspto-grants-2015_07