Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1747082Generated: November 1, 2026

Pentamethylbenzene → HCID 72303454, compound

https://huagongshe.com/reaction/1747082

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPentamethylbenzeneHCID 12784—
ReactantHCID 72303507HCID 72303507—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 72303454HCID 7230345499.9%

Reaction Steps

A solution of 400 mg of (3RS,4RS)-6-(benzyloxy)-3-(2,4-dichlorophenyl)-2-{(1SR,2SR)-2-[(methylsulfonyl)amino]cyclohexyl}-1-oxo-N-(pyridin-2-ylmethoxy)-1,2,3,4-tetrahydroisoquinoline-4-carboxamide and 245 mg of pentamethylbenzene in 15 ml of trifluoroacetic acid was stirred at room temperature overnight. The trifluoroacetic acid was evaporated under reduced pressure, and ethyl acetate and water were added thereto to carry out a liquid separation operation. The organic layer was washed with a saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate, and then evaporated under reduced pressure. The residue was solidified with ethyl acetate-isopropyl alcohol and collected by filtration to obtain 350 mg of (3RS,4RS)-3-(2,4-dichlorophenyl)-6-hydroxy-2-{(1SR,2SR)-2-[(methylsulfonyl)amino]cyclohexyl}-1-oxo-N-(pyridin-2-ylmethoxy)-1,2,3,4-tetrahydroisoquinoline-4-carboxamide as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150541B2
Source datasetuspto-grants-2015_10
ORD IDord-4c8c56940e6f430f892c3304b929bbe9
Source noteuspto-grants-2015_10