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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2196648Generated: October 29, 2026

Nitromethane → HCID 86653260, compound

https://huagongshe.com/reaction/2196648

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitromethaneHCID 6375—
ReactantChloroacetyl chlorideHCID 6577—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant2,6-difluoro-3-(propylsulfonamido)-N-(1H-pyrrolo[2,3-b]pyridin-5-yl)benzamideHCID 44199408—
SolventDichloromethaneHCID 6344—
SolventAmmonium ChlorideHCID 25517—
ProductHCID 86653260HCID 8665326050%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of aluminum trichloride (0.266 g, 2.00 mmol) in 1:1 DCM:CH3NO2 (5 mL) was added slowly to a slurry of 2,6-difluoro-3-(propylsulfonamido)-N-(1H-pyrrolo[2,3-b]pyridin-5-yl)benzamide (0.100 g, 0.254 mmol) in 1:1 DCM:CH3NO2 (2 mL) at 0° C. The solution was stirred at 0° C. for 40 minutes. A solution of 2-chloroacetyl chloride (0.0307 mL, 0.380 mmol) in DCM (1 mL) was added, and the reaction mixture was allowed to warm to room temperature overnight. Additional 2-chloroacetyl chloride (5 eq.) was added, and the reaction mixture was warmed to 50° C. for 20 hours. The solution was cooled and diluted with saturated aqueous ammonium chloride and extracted with EtOAc (3 X). The organic layers were dried over Na2SO4, filtered and concentrated under reduced pressure. They were then purified via column chromatography (5% MeOH/DCM) to afford N-(3-(2-chloroacetyl)-1H-pyrrolo[2,3-b]pyridin-5-yl)-2,6-difluoro-3-(propylsulfonamido)benzamide (59 mg, 50%) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338452B2
Source datasetuspto-grants-2012_12
ORD IDord-8ba30353c9bd4c4391a00059310848a0
Source noteuspto-grants-2012_12