Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1261936Generated: November 2, 2026

m-Chloroperbenzoic acid → 7-Bromo-2-(methylsulfinyl)pyrrolo[2,1-f][1,2,4]triazine

https://huagongshe.com/reaction/1261936

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant7-Bromo-2-(methylsulfanyl)pyrrolo[2,1-f][1,2,4]triazineHCID 57416128—
SolventDichloromethaneHCID 6344—
Product7-Bromo-2-(methylsulfinyl)pyrrolo[2,1-f][1,2,4]triazineHCID 5807130776.7%

Reaction Steps

Into a Round bottom flask, 7-Bromo-2-methylsulfanyl-pyrrolo[2,1-f][1,2,4]triazine (4.00 g, 0.0164 mol) and Methylene chloride (100 mL) were added. m-Chloroperbenzoic acid (77% max)(5.14 g, 0.0229 mol) was added portion wise over 20 minutes and the reaction was stirred at room temperature for one hour. The mixture was partitioned with DCM (200 mL) and saturated NaHCO3 (200 mL). Organic extracts were 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 afford 3.27 grams of 7-Bromo-2-methanesulfinyl-pyrrolo[2,1-f][1,2,4]triazine as a yellow powder. 1H NMR (400 MHz, DMSO, d6) δ 9.34 (s, 1H), 7.51 (m, 1H), 7.41 (d, 1H, J=4.71 Hz), 3.43 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08471005B2
Source datasetuspto-grants-2013_06
ORD IDord-3cbe75ad90dd40689b057ff82079cc51
Source noteuspto-grants-2013_06