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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1910528Generated: October 26, 2026

Benzenemethanamine, 3-chloro- → t-Butyl 4-(5-(3-chlorobenzylamino)-2-nitrophenyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1910528

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenemethanamine, 3-chloro-HCID 77802—
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-Butyl 4-(5-Fluoro-2-nitrophenyl)piperazine-1-carboxylateHCID 22272537—
SolventAcetonitrileHCID 6342—
Productt-Butyl 4-(5-(3-chlorobenzylamino)-2-nitrophenyl)piperazine-1-carboxylateHCID 5870731048%

Reaction Steps

t-Butyl 4-(5-fluoro-2-nitrophenyl)piperazine-1-carboxylate (431 mg, 1.3 mmol), 3-chlorobenzylamine (187 mg, 1.3 mmol), N,N-diisopropylethylamine (342 mg, 1.3 mmol) were stirred at 80° C. in dry acetonitrile (25 mL) for 72 h. The solvent was evaporated and the residue was dissolved in dichloromethane and washed with water. The dichloromethane was evaporated and the crude compound was purified by silica chromatography using 25% ethyl acetate in hexanes to afford the title compound (277 mg, 48% yield). 1H NMR (400 MHz, CD3OD): δ 7.96 (d, 1H), 7.37-7.26 (m, 4H), 6.29 (d, 1H), 6.18 (s, 1H), 4.42 (s, 2H), 3.55 (m, 4H), 2.92 (m, 4H), 1.47 (s, 9H); MS (ESI) m/z: Calculated for C22H27ClN4O4: 446.17; Observed: 469.2 (M++Na).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604021B2
Source datasetuspto-grants-2013_12
ORD IDord-230103ab97064207a912fd21b7ff15b4
Source noteuspto-grants-2013_12