Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1263396Generated: November 1, 2026

(4-Nitrophenyl)acetic acid → HCID 22594953, compound

https://huagongshe.com/reaction/1263396

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Nitrophenyl)acetic acidHCID 4661—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
Reactant3-(4-Bromo-1-Methyl-1H-Pyrazol-3-Yl)AnilineHCID 2735391—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
SolventChloroformHCID 6212—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 22594953HCID 2259495318.1%

Reaction Steps

A mixture of 3-(3-aminophenyl)-4-bromo-1-methylpyrazole (30 mg, 0.12 mmol), 4-nitrophenylacetic acid (22 mg, 0.12 mmol), 1-hydroxybenzotriazole hydrate (16 mg, 0.12 mmol) and 2-(1H-benzotriazole-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate (46 mg, 0.12 mmol) were dissolved in chloroform (1.5 ml). N, N-Diisopropylethylamine (0.02 ml, 0.13 mmol) was added and the mixture stirred at room temperature for 16 h. The reaction mixture was then poured into brine and the organic layer washed with further brine, dried over magnesium sulphate and then concentrated in vacuo. The crude product was purified by column chromatography (ethyl acetate-toluene, 1:1), giving the title compound (9 mg, 18%). Rf 0.19 (ethyl acetate-toluene, 1:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06541209B1
Source datasetuspto-grants-2003_04
ORD IDord-e2ae058efede4c3e81f0d48d3b581a06
Source noteuspto-grants-2003_04