HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 719632Generated: October 29, 2026
Methylamine → 2-Chloro-5-[3-(methylamino)propyl]-N-(tricyclo[3.3.1.13,7]dec-1-ylmethyl)-benzamide, acetate salt
https://huagongshe.com/reaction/719632
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | chloro-5-[3-[(methylsulfonyl)oxy]propyl]-N-(tricyclo[3.3.1.13,7]dec-1-ylmethyl)-benzamide | HCID 12988688 | — |
| Product | 2-Chloro-5-[3-(methylamino)propyl]-N-(tricyclo[3.3.1.13,7]dec-1-ylmethyl)-benzamide, acetate salt | HCID 10224916 | — |
Reaction Steps
Methylamine (2M tetrahydrofuran, 8 ml) was added to 2-chloro-5-[3-[(methylsulfonyl)oxy]propyl]-N-(tricyclo[3.3.1.13,7]dec-1-ylmethyl)-benzamide (0.250 g, Example 6e) and heated in a sealed tube at 70° C. for 18 h. On cooling to ambient temperature, the solution was diluted with ethyl acetate and extracted twice with saturated sodium hydrogencarbonate solution and once with brine, dried over magnesium sulfate and concentrated under reduced pressure. Purification by preparative reverse phase HPLC (eluting with a gradient of acetonitrile in 0.1% aqueous ammonium acetate/25–95%) gave the title compound as the acetate salt (0.140 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07132457B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-eb6129af4ddc4a4fb30abb3afe68b78c |
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| Source note | uspto-grants-2006_11 |
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