HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393208Generated: October 29, 2026
4-Morpholinecarbonyl chloride → HCID 22649548, compound
https://huagongshe.com/reaction/393208
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Morpholinecarbonyl chloride | HCID 84810 | — |
| Reactant | (7-Bromo-1,2,3,4-tetrahydro-naphthalen-2-yl)-piperidin-4-yl-propyl-amine | HCID 22649540 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Diisopropylethylamine | HCID 81531 | — |
| Product | HCID 22649548 | HCID 22649548 | — |
Reaction Steps
To a solution of the (7-bromo-1,2,3,4-tetrahydro-naphthalen-2-yl)-piperidin-4-yl-propyl-amine (200 μL of 0.25 M in dichloromethane, 50 μmol) was added 220 μL of 0.25 M solution of morpholine 4-carbonyl chloride in dichloromethane and 30 μL of DIEA. The reaction was stirred at 25° C. for 24 h. Concentrated in vacuo. The final product was isolated by preparative RPHPLC (YMC Combiprep ODS-A column, 10-90% acetonitrile: water (0.1% TFA)) to afford {4-[(7-bromo-1,2,3,4-tetrahydro-naphthalen-2-yl)-propyl-amino]-piperidin-1-yl}-pyrrolidin-1-yl-methanone 34 (4.6 mg), [M+H]+=562.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06806278B2 |
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| Source dataset | uspto-grants-2004_10 |
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| ORD ID | ord-4386ef212d414d569c2c5f6d3288801c |
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| Source note | uspto-grants-2004_10 |
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