HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1532327Generated: October 31, 2026
Phenylethanolamine → 5-(N-(2-Hydroxy-2-phenylethyl)-2-aminoethyl)amino-2-chloro-N-(tricyclo[3.3.1.13,7]dec-1-ylmethyl)-benzamide
https://huagongshe.com/reaction/1532327
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phenylethanolamine | HCID 1000 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Chloro-5-(2-chloroethyl)amino-N-(tricyclo[3.3.1.13,7]dec-1-ylmethyl)benzamide | HCID 11417653 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-(N-(2-Hydroxy-2-phenylethyl)-2-aminoethyl)amino-2-chloro-N-(tricyclo[3.3.1.13,7]dec-1-ylmethyl)-benzamide | HCID 20670037 | 34.8% |
Reaction Steps
2-Chloro-5-(2-chloroethyl)amino-N-(tricyclo[3.3.1.13,7]dec-1-ylmethyl)benzamide from Example 63 (0.1 g), 2-amino-1-phenylethanol (0.539 g) and triethylamine (0.5 ml) were dissolved in tetrahydrofuran (3 ml) and heated at 80° C. for 60 hours in a sealed tube. The reaction mixture was concentrated under reduced pressure, the residue was suspended in aqueous sodium hydrogen carbonate (30 ml), the product was extracted into ethyl acetate (3×30 ml), dried over magnesium sulphate filtered and concentrated under reduced pressure. Purification by NPHPLC eluting with 0 to 25% ethanol in dichloromethane gave title compound as a white solid (0.044 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06201024B1 |
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| Source dataset | uspto-grants-2001_03 |
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| ORD ID | ord-b9cd7a06e44e46adb1dd6f4bc6ee9eda |
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| Source note | uspto-grants-2001_03 |
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