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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 272247Generated: October 30, 2026

Phenylhydrazine → HCID 178504821, compound

https://huagongshe.com/reaction/272247

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylhydrazineHCID 7516—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 178504822HCID 178504822—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductHCID 178504821HCID 17850482151.3%

Reaction Steps

A solution of 0.3 g (0.441 mmol) of trans-4-[4-(benzyl{(2S)-3-[4-(benzyloxy)-3-(methylsulfonyl)phenoxy]-2-hydroxypropyl}amino)cyclohexyl]benzoic acid (preparation 4), of 0.78 g (0.91 mmol) of 1-hydroxybenzotriazole, of 0.169 g (0.88 mmol) of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride, of 0.184 ml of triethylamine and of 0.095 g (0.88 mmol) of phenylhydrazine in a mixture of 4 ml of dichloromethane and 0.8 ml of acetonitrile is stirred for 48 hours. The solvents are evaporated under reduced pressure. Dichloromethane and water are added and the organic phase is washed three times with water. The organic phases are dried over magnesium sulfate and concentrated under reduced pressure. The product is obtained in the form of a white solid (0.166 g, 50%) after purification on silica gel (eluent: heptane/ethyl acetate 60/40 for 10 min, 60/40 to 40/60 in 10 min, then 40/60 for 20 min gradient). [M+H+]=734.7

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07453010B2
Source datasetuspto-grants-2008_11
ORD IDord-1c15759c60054917a4347a7e03ed6a8b
Source noteuspto-grants-2008_11