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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1261899Generated: November 2, 2026

Dichloromethane → HCID 66711241, compound

https://huagongshe.com/reaction/1261899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 66711390HCID 66711390—
ProductHCID 66711241HCID 6671124186%

Reaction Steps

Into a Round bottom flask, [A] 5-Bromo-2-methylsulfanyl-7-phenyl-pyrrolo[2,1-f][1,2,4]triazine (0.30 g, 0.00094 mol) and Methylene chloride (2 mL, 0.03 mol) were added. m-Chloroperbenzoic acid (0.178 g, 0.00103 mol) was added portion wise over 20 minutes. The reaction was stirred at room temperature for one hour. The reaction was partitioned with DCM (200 mL) and saturated NaHCO3 (200 mL). The organic was separated, washed with Brine and dried over Na2SO4. The solid was filtered and washed with DCM. The solvent was removed under vacuum to give a yellow solid. The solid was washed with hexane to give 5-Bromo-2-methanesulfinyl-7-phenyl-pyrrolo[2,1-f][1,2,4]triazine as a yellow solid (270 mg, 86%). NMR 1H (DSMO-d6)-9.24 (s, 1H), 8.24 (d, 2H, J=7.44 Hz), 7.92 (s, 1H), 7.56 (t, 2H, J=7.93 Hz), 7.47 (t, 1H, J=7.32 Hz), 2.98 (s, 3H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08471005B2
Source datasetuspto-grants-2013_06
ORD IDord-24dfddab36b544ac97e4087cb9d3f77b
Source noteuspto-grants-2013_06