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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1369556Generated: October 30, 2026

1-Hydroxybenzotriazole → N-[2-methyl-5-(3-morpholinobenzamido)phenyl]-3-tetrahydrofuran-3-yloxybenzamide

https://huagongshe.com/reaction/1369556

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantN-(3-amino-4-methylphenyl)-3-morpholinobenzamideHCID 11301391—
Reactant3-(Tetrahydrofuran-3-yloxy)benzoic acidHCID 22291089—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductN-[2-methyl-5-(3-morpholinobenzamido)phenyl]-3-tetrahydrofuran-3-yloxybenzamideHCID 2229105863.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (0.165 g) was added to a stirred mixture of 3-(tetrahydrofuran-3-yloxy)benzoic acid (0.15 g), 1-hydroxybenzotriazole (0.146 g) and DMF (5 ml) which had been cooled to 0° C. The reaction mixture was stirred at 0° C. for 5 minutes and a solution of N-(3-amino-4-methylphenyl)-3-morpholinobenzamide (0.224 g) in DMF (1 ml) was added. The reaction mixture was allowed to come to ambient temperature and was stirred for 16 hours. The reaction mixture was poured into water and the resultant solid was isolated and purified by column chromatography on silica using a 99:1 mixture of methylene chloride and methanol as eluent. There was thus obtained the title compound (0.228 g); NMR Spectrum: (DMSOd6) 1.99 (m, 1H), 2.18 (s, 3H), 2.25 (m, 1H), 3.17 (t, 4H), 3.72 (t, 4H), 3.88 (m, 4H), 5.13 (m, 1H), 7.11 (m, 2H), 7.21 (d, 1H), 7.39 (m, 5H), 7.56 (m, 2H), 7.79 (m, 2H), 9.83 (s, 1H), 10.11 (s, 1H); Mass Spectrum: M+H+502.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06579872B1
Source datasetuspto-grants-2003_06
ORD IDord-b4972646a5fc4f4dbc4ba5cadbbc8dc6
Source noteuspto-grants-2003_06