HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1355381Generated: October 25, 2026
Sodium Bicarbonate → N-[(S)-2-(3,4-Dichlorophenyl)-4-hydroxybutyl]-N-methyl-3-cyano-1-naphthamide
https://huagongshe.com/reaction/1355381
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (gammaS)-gamma-(Aminomethyl)-3,4-dichlorobenzenepropanol | HCID 20794251 | — |
| Reactant | 3-Cyano-1-naphthoyl chloride | HCID 22636686 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-[(S)-2-(3,4-Dichlorophenyl)-4-hydroxybutyl]-N-methyl-3-cyano-1-naphthamide | HCID 53679342 | 78% |
Reaction Steps
(S)-2-(3,4-Dichlorophenyl)-4-hydroxybutylamine (20.8 g, 83.8 mmol) was dissolved in DCM (700 mL). To the stirred solution was added 10% aqueous sodium bicarbonate (300 mL), and the mixture cooled to 0° C. A solution of 3-cyano-1-naphthoyl chloride (17.4 g, 80.6 mmol) in DCM (300 mL) was added dropwise over 30 minutes. The mixture was then allowed to warm to ambient temperature and stir for 20 h. The layers were separated, and the aqueous phase washed with DCM (300 mL). The combined organic layers were dried (Na2SO4), filtered, and evaporated in vacuo to give a white foam. Purification by chromatography (silica gel; 0-25% acetonitrile in DCM) provided the desired product as a white foam (27.0 g, 78%). 1H-NMR (DMSO-d6) δ1.46-1.60 (m, 1H, CH); 1.77-1.91 (m, 3H, CH); 4.38-4.41 (t, 1H, CH); 4.54-4.57 (t, 2H, CH); 6.43 (broad, 1H, OH); 6.84-7.26 (m, 2H, aromatic); 7.44-7.54 (m, 3H, aromatic); 7.57-7.80 (m, 7H, aromatic); 8.04-8.33 (m, 2H, aromatic); 8.61 (s, 1H, aromatic).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06586432B2 |
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| Source dataset | uspto-grants-2003_07 |
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| ORD ID | ord-4ad19378555c4a838fd6174da7082420 |
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| Source note | uspto-grants-2003_07 |
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