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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080241Generated: October 31, 2026

Toluene → HCID 178512316, compound

https://huagongshe.com/reaction/2080241

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantBenzyl BromideHCID 7498—
ReactantCyanamideHCID 9864—
ReactantHCID 58875330HCID 58875330—
SolventTrifluoroacetic acidHCID 6422—
SolventN-methyl-2-pyrrolidoneHCID 13387—
SolventAcetonitrile--water (1/1)HCID 18373917—
ProductHCID 178512316HCID 1785123164.5%

Reaction Steps

To a mixture of quinoline-6-carbothioic acid 4-benzyloxy-benzylamide described in Preparation Example E+-10 (57 mg, 0.15 mmol) and toluene (2 mL) was added benzyl bromide (0.089 mL, 0.74 mmol), which was then stirred under reflux for 90 minutes. After cooling, the solvent was evaporated in vacuo, and the residue was washed with diethyl ether twice. A mixture of a portion (16 mg) of the resulting crude product (72 mg), cyanamide (20 mg, 0.48 mmol) and N-methylpyrrolidinone (1 mL) was stirred for 2.5 hours at 120° C. After cooling, the reaction solution was filtered through a membrane filter, the filtrate was directly purified by reverse phase high performance liquid chromatography (acetonitrile-water mobile phase (containing 0.1% trifluoroacetic acid) was used), and trifluoroacetic acid salt of the title compound (0.76 mg, 0.0015 mmol, 4.5%) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932272B2
Source datasetuspto-grants-2011_04
ORD IDord-771b2f3a6a984a46a3e368d2ed2a8494
Source noteuspto-grants-2011_04