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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1163071Generated: October 28, 2026

Oxalyl chloride → HCID 25032264, compound

https://huagongshe.com/reaction/1163071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-(Dimethylamino)pyrrolidineHCID 2758519—
ReactantHCID 58970773HCID 58970773—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 25032264HCID 25032264—

Reaction Steps

The 4-(2-phenyl-benzoimidazol-1-ylmethyl)-benzoic acid (0.2 mmol) obtained in step 2 is dissolved in DCM (5 mL) and oxalylchloride (0.2 mL, 0.4 mmol, 2 M solution in DCM) and DMF (2 drops) are added. The solution is stirred for 2 hours at room temperature then concentrated in vacuo. The residue is dissolved in THF, treated with diisopropylethylamine (DIEA) (0.09 mL, 0.5 mmol) and 3-(dimethylamino)pyrrolidine (0.22 mmol, 22 uL), stirred at room temperature overnight then concentrated. This residue is dissolved in a mixture of DMSO, MeOH and water (1.5 mL) and purified by reverse-phase semi-preparative HPLC1 to the title product as a white powder (13 mg), identified by HPLC2 and MS [425.2 m/e (M+H)].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820825B2
Source datasetuspto-grants-2010_10
ORD IDord-094c54ae3454423e82fe5176359422b3
Source noteuspto-grants-2010_10