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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1941894Generated: October 31, 2026

1,2-Dichloroethane → HCID 58504345, compound

https://huagongshe.com/reaction/1941894

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantTriethylamineHCID 8471—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant5-Amino-1-phenyl-1H-pyrazole-4-carboxylic acidHCID 746814—
ReactantHCID 58504342HCID 58504342—
SolventDimethylformamideHCID 6228—
ProductHCID 58504345HCID 5850434552.2%

Reaction Steps

A mixture of 5-amino-1-phenyl-1H-pyrazole-4-carboxylic acid (90 mg, 0.441 mmol), (Z)-methyl 1-(4-(N′-hydroxycarbamimidoyl)benzyl)azetidine-3-carboxylate (116 mg, 0.441 mmol), EDC (84 mg, 0.441 mmol) and HOBT (67.5 mg, 0.441 mmol) in DMF (1 mL) was stirred at RT for 1 hr. At this time, Et3N (0.061 mL, 0.441 mmol) was added and stirring was continued at RT for 3 days. The mixture was then heated to 50° C. for 10 minutes. The reaction mixture was partitioned between EtOAc (30 mL) and saturated sodium bicarbonate solution (30 mL). The organic layer was washed with saturated sodium bicarbonate solution (30 mL), water (30 mL) and brine (30 mL). After drying (MgSO4) and filtration, the organic layer was concentrated to afford (Z)-methyl 1-(4-(N′-(5-amino-1-phenyl-1H-pyrazole-4-carbonyloxy)carbamimidoyl)benzyl)azetidine-3-carboxylate (103 mg, 0.230 mmol) as a white solid. HPLC retention time=1.05 minutes (PHENOMENEX® Luna 4.6×30 mm S-5 ODS column) eluting with 10-90% aqueous methanol+0.1% TFA over a 2 minute gradient. MS:(M+H)=449.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08389509B2
Source datasetuspto-grants-2013_03
ORD IDord-340d26b303cb4f0bb5f8ecd054fc98c3
Source noteuspto-grants-2013_03