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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (S)-3-amino-5-(4-methylpiperazin-1-yl)-1,4-dihydro-2H-1-benzopyran | HCID 11139461 | — |
| Reactant | 4-(Morpholin-4-yl)benzene-1-sulfonyl chloride | HCID 14951211 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (S)-N-[5-(4-Methylpiperazin-1-yl)-3,4-dihydro-2H-1-benzopyran-3-yl]-4-morpholinobenzenesulfonamide | HCID 69210902 | 61.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06479497B1 |
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| Source dataset | uspto-grants-2002_11 |
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| ORD ID | ord-6862803762b149209c71299fa3015e93 |
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| Source note | uspto-grants-2002_11 |
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