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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1505633Generated: October 31, 2026

N-bromobutanimide → HCID 66671334, compound

https://huagongshe.com/reaction/1505633

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 16222885HCID 16222885—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66671334HCID 66671334—

Reaction Steps

To a solution of benzyl-(3-p-tolyl-thieno[3,2-c]pyridin-4-yl)-amine (314 mg, 0.984 mmol), in THF (5 ml) cooled to 0° C., was added N-bromosuccinimide (168 mg, 0.984 mmol) and the reaction stirred for 1.5 h. The reaction was then allowed to warm to room temperature and the solvent removed in vacuo. The crude residue was partitioned between NH4Cl (25 ml) and DCM (10 ml), the organic layer dried (MgSO4) and the solvent removed in vacuo. No further purification was required. The product was obtained as a yellow solid (390 mg, quantitative).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216992B2
Source datasetuspto-grants-2015_12
ORD IDord-33c73a17f484458ea95b45238745f536
Source noteuspto-grants-2015_12