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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1477284Generated: November 2, 2026

Diclofenac → Diclofenac lactam

https://huagongshe.com/reaction/1477284

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiclofenacHCID 3033—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactanttert-butyl N-(2-hydroxyethyl)carbamateHCID 2733206—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductDiclofenac lactamHCID 27211—
Product[2-(2,6-Dichloro-phenylamino)-phenyl]-acetic acid 2-tert-butoxycarbonylamino-ethyl esterHCID 118302985—

Reaction Steps

To a stirred solution of [2-(2,6-Dichloro-phenylamino)-phenyl]-acetic acid] 2 (4.0 g, 0.01 mol, 1 eq) and N—BOC-Ethanolamine (2.39 g, 0.01 mol) in DCM (70 mL) was added DMAP (0.16 g, 0.001 mol) at rt. To this mixture was added DCC (5.5 g, 0.02 mol) in DCM (30 mL) drop-wise at 0-5° C. and resulting mixture was stirred at room temperature for 1 h. Reaction was monitored by TLC. After completion, reaction mixture was filtered and the solvent was removed under reduced pressure. Residue was dissolved in water (100 mL) and extracted with DCM (2×50 mL). Combined organic layer was dried over anhydrous Na2SO4 and evaporated under reduced pressure to obtained crude compound which was washed with hexane (2×20 mL), dried to get 6.0 g crude of Compound 4 and cyclized compound 1 as an off white solid. This mixture was used in the next step without any further purification; Mass: 439.3 (M++H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403793B2
Source datasetuspto-grants-2016_08
ORD IDord-9e8a621716bd43eca7ba2fe890d9ccf5
Source noteuspto-grants-2016_08