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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 575672Generated: October 29, 2026

4-(2-Fluoro-5-methylsulfonylphenyl)-2-methylisoquinolin-1-one → HCID 178480092, compound

https://huagongshe.com/reaction/575672

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(2-Fluoro-5-methylsulfonylphenyl)-2-methylisoquinolin-1-oneHCID 118021901—
ReactantHCID 178511715HCID 178511715—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 178480092HCID 17848009229%

Reaction Conditions

Temperature250 °C

Reaction Steps

A mixture of 4-(2-fluoro-5-methylsulfonylphenyl)-2-methylisoquinolin-1-one (150 mg, 0.45 mmol) and trans-4-aminocyclohexan-1-ol (417 mg, 3.62 mmol) in NMP (0.2 mL) was heated for 20 min at 200-300° C. The cooled brownish residue was purified by prep-HPLC to give the title compound (55.64 mg, 28.8%) as a yellow solid. 1H NMR (CDCl3, 400 MHz) δ 8.54 (d, J=8.0 Hz, 1H), 7.86 (dd, J1=8.8 Hz, J2=2.4 Hz, 1H), 7.66 (d, J=2.4 Hz, 1H), 7.60-7.55 (m, 2H), 7.15-7.13 (m, 2H), 6.79 (d, J=8.8 Hz, 1H), 3.91-3.85 (m, 1H), 3.67 (s, 3H), 3.63-3.55 (m, 1H), 3.37-3.34 (m, 1H), 3.06 (s, 3H), 2.04-1.92 (m, 5H), 1.44-1.35 (m, 2H), 1.11-1.02 (m, 2H). LCMS (M+H)+=427.1 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09034900B2
Source datasetuspto-grants-2015_05
ORD IDord-94d17a31841448938249d38c5e90cce7
Source noteuspto-grants-2015_05