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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1017608Generated: October 29, 2026

Triethylamine → (S)-N-[5-(4-Methylpiperazin-1-yl)-3,4-dihydro-2H-1-benzopyran-3-yl]-4-morpholinobenzenesulfonamide

https://huagongshe.com/reaction/1017608

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant(S)-3-amino-5-(4-methylpiperazin-1-yl)-1,4-dihydro-2H-1-benzopyranHCID 11139461—
Reactant4-(Morpholin-4-yl)benzene-1-sulfonyl chlorideHCID 14951211—
SolventDichloromethaneHCID 6344—
Product(S)-N-[5-(4-Methylpiperazin-1-yl)-3,4-dihydro-2H-1-benzopyran-3-yl]-4-morpholinobenzenesulfonamideHCID 6921090261.5%

Reaction Steps

To a solution of (S)-3-amino-5-(4-methylpiperazin-1-yl)-3,4-dihydro-2H-1-benzopyran (120 mg, 0.485 mmol) in anhydrous methylene chloride (10 mL) were added triethylamine (81 μL, 0.582 mmol) and 4-(4-morpholinyl)benzenesulfonyl chloride (140 mg, 0.534 mmol; described in: Galliani, G. Eur. Pat. Appl. EP 335,758, 1989, Chem. Abstr. 1990, 112, 98374d [125393-22-8]). The reaction mixture was stirred at room temperature for 4 h, washed with a 2 M NH3 solution, dried (MgSO4) and concentrated in vacuo. The crude product was purified by column chromatography on silica (eluent: chloroform/ethanol, 90:10+0.5% conc. NH3) affording 141 mg (61% yield) of the title compound as a white solid: mp sinters>100° C.; [α]22D+10° (c 1.0, chloroform); EIMS (70 eV) m/z (relative intensity) 472 (56, M30 ).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06479497B1
Source datasetuspto-grants-2002_11
ORD IDord-6862803762b149209c71299fa3015e93
Source noteuspto-grants-2002_11