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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2200060Generated: October 26, 2026

Dichloromethane → 3-Chloro-6-fluoro-[1,2,4]triazolo[4,3-a]pyridine

https://huagongshe.com/reaction/2200060

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantN-bromobutanimideHCID 67184—
Reactant6-Fluoro-[1,2,4]triazolo[4,3-a]pyridineHCID 55267245—
Product3-Chloro-6-fluoro-[1,2,4]triazolo[4,3-a]pyridineHCID 5526754063%

Reaction Conditions

Temperature45 °C

Reaction Steps

Intermediate 14a (908 mg, 6.60 mmol) was dissolved in DCM (50 mL) and N-bromosuccinimide (1.29 g, 7.26 mmol) added. The reaction was heated to 45° C. for 4 h, then cooled and partitioned between DCM (150 mL) and saturated aqueous NaHCO3 (150 mL), and extracted into DCM (3×). The combined organic layers were washed with brine, dried (MgSO4) and evaporated in vacuo. Purification by FCC, using 0-5% [2M NH3 in MeOH] in DCM, gave the title compound (900 mg, 63%). LCMS (Method 1): Rt 1.94 min, m/z 216/218 [MH+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359354B2
Source datasetuspto-grants-2016_06
ORD IDord-f5529c36dcaf4e95aa67545b3d220c5b
Source noteuspto-grants-2016_06