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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1778313Generated: October 30, 2026

Triethylamine → HCID 118329947, compound

https://huagongshe.com/reaction/1778313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantN,N'-Di-Boc-thioureaHCID 5193990—
ReactantHCID 118323976HCID 118323976—
SolventDimethylformamideHCID 6228—
ProductHCID 118329947HCID 118329947—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a mixture of 6-(bis(4-chlorophenyl)methyl)-4-(piperidin-4-ylamino)quinolin-2(1H)-one (250 mg, 0.523 mmol0, N,N′-bis-tert-butoxycarbonylthiourea (158.8 mg, 0.575 mmol) and triethylamine (0.22 mL, 1.57 mmol) in 3 mL DMF was added mercuric chloride (170.2 mg, 0.63 mmol) at 0° C. The reaction was stirred for 3 h at 0° C. and then quenched with EtOAc. The reaction was filtered through CELITE. The filtrate was washed two times with water, then dried over anhydrous Na2SO4, filtered and concentrated. The resulting residue was purified on ISCO with MeOH—CH2Cl2 and re-purified on HPLC (40-90% CH3CN (0.1% TFA)/H2O (0.1% TFA)) to yield (Z)-tert-butyl ((4-((6-(bis(4-chlorophenyl)methyl)-2-oxo-1,2-dihydroquinolin-4-yl)amino)piperidin-1-yl)((tert-butoxycarbonyl)imino)methyl)carbamate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266835B2
Source datasetuspto-grants-2016_02
ORD IDord-f01628f2a5cb4bb192f628ce8d877cf1
Source noteuspto-grants-2016_02