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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1357229Generated: November 1, 2026

Chloride → HCID 69138517, compound

https://huagongshe.com/reaction/1357229

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorideHCID 312—
ReactantTriethylamineHCID 8471—
Reactant1-Phenyl-5-propyl-1H-pyrazole-4-carbonyl chlorideHCID 3775717—
ReactantHCID 18505313HCID 18505313—
SolventDichloromethaneHCID 6344—
ProductHCID 69138517HCID 6913851795%

Reaction Steps

Triethylamine (0.192 mL, 1.38 mmol) was added under nitrogen to a mixture of 5-bromo-6-methoxycarbonylmethoxy-naphthalen-2-ylmethyl-ammonium; chloride (0.25 g, 0.69 mmol), prepared in the previous step, and 1-phenyl-5-propyl-1H-pyrazole-4-carbonyl chloride (0.17 g, 0.69 mmol) in 20 mL of methylene chloride at room temperature. The reaction stirred under nitrogen for 17 h. The reaction was diluted with methylene chloride, extracted two times with water, two times with 5% sodium bicarbonate, dried (MgSO4) and the solvent removed under reduced pressure to give (1-Bromo-6-{[(1-phenyl-5-propyl-1H-pyrazole-4-carbonyl)-amino]-methyl}-naphthalen-2-yloxy)-acetic acid methyl ester (0.347 g, 95%) as a white solid, mp 144-146° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06589970B2
Source datasetuspto-grants-2003_07
ORD IDord-b8dc005596b644aaa94d224b79ab2339
Source noteuspto-grants-2003_07