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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2370989Generated: October 31, 2026

Dimethyl Sulfide → HCID 51347785, compound

https://huagongshe.com/reaction/2370989

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfideHCID 1068—
ReactantBoron trifluorideHCID 6356—
ReactantHCID 67108944HCID 67108944—
CatalystMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 51347785HCID 5134778527.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

2-(3,5-dimethylisoxazol-4-yl)-3-(4-methoxyphenyl)-N,N-dimethyl-1H-indole-1-sulfonamide (23 mg, 0.05 mmol) was dissolved in DCM and the mixture was cooled at 0° C. BF3.SMe2 (0.7 ml) was added drop wise and the reaction mixture was stirred in the fridge for 16 h. A few drops MeOH were added to the cool mixture. The mixture was then extracted with H2O/DCM using an isolute phase separator. Concentration gave a crude product which was purified using HPLC (40-70% AcN, 25 min gradient). 5.6 mg 2-(3,5-dimethylisoxazol-4-yl)-3-(4-hydroxyphenyl)-N,N-dimethyl-1H-indole-1-sulfonamide was obtained. ES/MS m/z: 412.06 (M+H), 410.16 (M−H); 1H NMR (acetone-d6, 500 MHz): 8.18 (m, 1H), 7.60 (m, 1H), 7.43 (m, 1H), 7.34 (m, 1H), 7.12 (m, 2H), 6.88 (m, 2H), 2.70 (s, 6H), 2.10 (s, 3H) and 2.09 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710243B2
Source datasetuspto-grants-2014_04
ORD IDord-cb4b8f66435244d881dd0ab4a3c169a1
Source noteuspto-grants-2014_04