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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443379Generated: October 30, 2026

Acetic Acid → HCID 178451477, compound

https://huagongshe.com/reaction/1443379

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantAmmonium HydroxideHCID 14923—
Reactant3-(2-oxo-2-phenyl-ethylcarbamoyl)-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert butyl esterHCID 23570725—
SolventDiethyl EtherHCID 3283—
ProductHCID 178451477HCID 178451477—

Reaction Steps

The product prepared in Step A above (3.55 g, 9 mmol), NH4OAc (ammonium acetate) (20.8 g, 270 mmol) and AcOH (acetic acid) (30 mL) were combined at room temperature and the reaction mixture was warmed on a steam bath for about 3 hours. The reaction mixture was then cooled to room temperature and poured into an ice slurry mix (400 g). To this mixture was added concentrated ammonium hydroxide (50 mL) and ethyl ether. The layers were separated, and the aqueous phase washed with a second portion of ethyl ether. The organic phases were combined, dried over MgSO4, filtered, and concentrated under reduced pressure to yield a brown foam. This sample was purified by preparative HPLC to yield the purified title compound as a white powder. LC indicated the sample was 96% pure at 214 nm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07659402B2
Source datasetuspto-grants-2010_02
ORD IDord-3cbd462d42b047bca53d3ddbbcda25b5
Source noteuspto-grants-2010_02