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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1726158Generated: November 2, 2026

Benzyl Bromide → HCID 68971366, compound

https://huagongshe.com/reaction/1726158

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantHCID 68973756HCID 68973756—
ProductHCID 68971366HCID 68971366—

Reaction Steps

Using general procedure H with the above aniline (970 mg, 1.81 mmol) and benzyl bromide (0.66 mL, 5.52 mmol) followed by general procedure C afforded N,N-dibenzyl-4-(benzyl-piperidin-4-yl-amino)-benzenesulfonamide as a white solid (679 mg, 72% over 2 steps).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491735B2
Source datasetuspto-grants-2009_02
ORD IDord-72d0aa757b3d43e48f4642975faeca89
Source noteuspto-grants-2009_02