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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1954741Generated: November 1, 2026

Dichloromethane → HCID 178459483, compound

https://huagongshe.com/reaction/1954741

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 178524941HCID 178524941—
CatalystDimethylformamideHCID 6228—
ProductHCID 178459483HCID 17845948363%

Reaction Steps

To a solution of 7-chloro-3-(carboxy)pyrazolo[3,4-c][1]benzazepine-4,10(1H,9H)-dione (500 mg, 1.7 mmol) (compound of Example 9) in dichloromethane (15 mL) was added N,N-dimethylformamide (2 drops) and then in one portion oxalyl chloride (300 μL, 3.4 mmol). The resulting solution was stirred for 24 hours at room temperature, concentrated by rotary evaporation, and allyl alcohol (15 mL) was added to the residue. The mixture was heated at 100° C. for 15 minutes and concentrated by rotary evaporation. The residue was purified by flash chromatography eluting with dichloromethane:methanol (95:5) to give the title compound as a solid (358 mg, 63% yield. 247-249° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06124281
Source datasetuspto-grants-2000_09
ORD IDord-f0abc53cc044445ba212dce47ba92f3b
Source noteuspto-grants-2000_09