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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 457341Generated: October 29, 2026

Allyl bromide → HCID 178513839, compound

https://huagongshe.com/reaction/457341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantHCID 22291714HCID 22291714—
SolventDimethylformamideHCID 6228—
ProductHCID 178513839HCID 178513839106.7%

Reaction Steps

To a stirring solution of the Cs+ salt of 1-{4-[(acetylamino)sulfonyl]phenyl}-8-[(2-chlorobenzoyl)amino]-4,5-dihydro-1H-benzo[g]indazole-3-carboxamide (637 mg, 0.92 mmol) in DMF (8 mL) was added a solution of allyl bromide (111 mg, 0.92 mmol). The solution was stirred at room temperature for over the weekend and concentrated. To the mixture was added MeOH—H2O (2:1). A precipitate was formed. It was filtered to give a yellow solid of 1-(4-[acetyl(allyl)amino]sulfonyl}phenyl)-8-[(2-chlorobenzoyl)amino]-4,5-dihydro-1H-benzo[g]indazole-3-carboxamide (360 mg, 65%.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07186743B2
Source datasetuspto-grants-2007_03
ORD IDord-bc67c705bceb42ec83775c5064742842
Source noteuspto-grants-2007_03