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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1779509Generated: November 2, 2026

1,2-Dichloroethane → 1-(4-Cyanobenzyl)imidazole-5-acetic acid

https://huagongshe.com/reaction/1779509

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantDimethylformamideHCID 6228—
Reactant4-MethylmorpholineHCID 7972—
Reactant3-hydroxy-1,2,3-benzotriazin-4(3H)-oneHCID 73026—
ReactantLithium ChlorideHCID 433294—
Reactant3(S)-ethyl-prolyl-methionine isopropyl ester hydrochlorideHCID 86750791—
Product1-(4-Cyanobenzyl)imidazole-5-acetic acidHCID 18433630—

Reaction Steps

LiCl (0.416 g, 1.47 mmol), pyrrolidin-2(S)-ylmethyl]-3(S)-ethyl-prolyl-methionine isopropyl ester hydrochloride (Step I) (0.63 g, 1.33 mmol), HOOBT (0.239 g, 1.47 mmol), and EDC (0.281 g, 1.47 mmol) were dissolved in degassed DMF (20 mL) with stirring at room temperature, N-methylmorpholine (0.8 mL, 5.32 mmol) was added to achieve a pH of 7, and stirring was continued overnight. The reaction mixture was concentrated to remove most of the DMF, and the residue was partitioned between EtOAc and aq satd NaHCO3 solution. The aq layer was washed with EtOAc, the organics combined, washed with brine and dried (MgSO4). Filtration and concentration to dryness gave the title compound after chromatography on silica gel eluting with CH2Cl2 :CH3OH, 95:5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05627202
Source datasetuspto-grants-1997_05
ORD IDord-3b4676f16ee14592a1f33649ee5ade90
Source noteuspto-grants-1997_05