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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1397935Generated: November 2, 2026

1-(3-Aminophenyl)ethanol → HCID 66762110, compound

https://huagongshe.com/reaction/1397935

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(3-Aminophenyl)ethanolHCID 222461—
ReactantHCID 66762693HCID 66762693—
ProductHCID 66762110HCID 66762110—

Reaction Steps

4-(N-(4-methoxyphenyl)-N-methylsulfamoyl)benzoic acid (7) (100 mg, 0.31 mmol) was treated with 1-(3-aminophenyl)ethanol (36 mg, 0.26 mmol) using method C. The residue was purified using flash chromatography eluting with 0-40% EtOAc in hexanes. The resulting solid was triturated with dichloromethane/hexanes to give N-(3-(1-hydroxyethyl)phenyl)-4-(N-(4-methoxyphenyl)-N-methylsulfamoyl)benzamide as an off white solid. Yield: 52 mg (46%). 1H-NMR: 10.45 (s, 1H), 8.12 (d, J=8.5 Hz, 2H), 7.75-7.74 (m, 1H), 7.68-7.64 (m, 3H), 7.30 (t, J=8.0 Hz, 1H), 7.10 (d, J=8.0 Hz, 1H), 7.01 (d, J=8.0 Hz, 2H), 6.90 (d, J=8.0 Hz, 2H), 5.19 (d, J=4.5 Hz, 1H), 4.75-4.68 (m, 1H), 3.75 (s, 3H), 3.15 (s, 3H), 1.33 (d, J=6.5 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901306B2
Source datasetuspto-grants-2014_12
ORD IDord-e11305212d294a81b66911c471b33bdf
Source noteuspto-grants-2014_12