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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 78371Generated: October 25, 2026

2-Morpholinoethylamine → 3-(4-Nitrophenoxy)benzoic acid

https://huagongshe.com/reaction/78371

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MorpholinoethylamineHCID 408285—
Reactant3-(4-Nitrophenoxy)benzoic acidHCID 767919—
Product3-(4-Nitrophenoxy)benzoic acidHCID 767919—
ProductN-[2-(4-morpholinyl)ethyl]-3-(4-nitrophenoxy)benzamideHCID 66745649—

Reaction Steps

Entry 61: 4-(3-Carboxyphenoxy)-1-nitrobenzene was synthesized according to Method A13, Step 2. 4-(3-Carboxyphenoxy)-1-nitrobenzene was coupled with 4-(2-aminoethyl)morpholine according to Method A13, Step 3 to give 4-(3-(N-(2-morpholinylethyl)carbamoyl)phenoxy)-1-nitrobenzene. According to Method A13 Step 4, 4-(3-(N-(2-morpholinylethyl)carbamoyl)phenoxy)-1-nitrobenzene was reduced to 4-(3-(N-(2-morpholinylethyl)carbamoyl)phenoxy)aniline. According to Method C1a, 4-chloro-3-(trifluoromethyl)phenyl isocyanate was reacted with 4-(3-(N-(2-morpholinylethyl)carbamoyl)phenoxy)aniline to afford the urea.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841330B2
Source datasetuspto-grants-2014_09
ORD IDord-4b915e102afe45c180e79fc45a756656
Source noteuspto-grants-2014_09