Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1424433Generated: October 25, 2026

2-Amino-4-(benzyloxy)benzamide → HCID 66610642, compound

https://huagongshe.com/reaction/1424433

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-4-(benzyloxy)benzamideHCID 23130277—
Reactant5-(4-Fluorophenyl)-1,3-dioxolane-2,4-dioneHCID 86649050—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66610642HCID 6661064264%

Reaction Conditions

Temperature63 °C

Reaction Steps

To a solution of 2-amino-4-(benzyloxy)benzamide (4.0 g, 16.5 mmol) in THF (60 mL) was added a solution of 5-(4-fluorophenyl)-1,3-dioxolane-2,4-dione (3.65 g, 18.6 mmol) from Example 16 in THF (20 mL) portionwise at rt. After heating to 63° C. for 18 h, the solution was cooled and concentrated. After addition of H2O, the solution was extracted twice with DCM. The combined organic phases were washed with brine and dried over sodium sulfate. Chromatography on silica gel eluting with 10 to 80% EtOAc/DCM afforded 4-(benzyloxy)-2-(2-(4-fluorophenyl)-2-hydroxyacetamido)benzamide as a foamy solid (4.1 g, 64%). 1H NMR (300 MHz, DMSO-d6) δ ppm 5.06 (m, 1H), 5.12 (s, 2H) 6.68-6.74 (m, 1H) 7.14-7.20 (m, 2H) 7.32-7.51 (m, 6H) 7.77 (d, J=8.85 Hz, 1H) 8.05 (br. s., 1H) 8.30 (d, J=2.64 Hz, 1H) 12.73 (s, 1H). LC-MS (ESI) m/z 392 (M−2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927711B2
Source datasetuspto-grants-2015_01
ORD IDord-573ce3e371224f49bf6b82baf5deb538
Source noteuspto-grants-2015_01