HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393204Generated: October 30, 2026
4-Morpholinecarbonyl chloride → HCID 10216398, compound
https://huagongshe.com/reaction/393204
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Morpholinecarbonyl chloride | HCID 84810 | — |
| Reactant | (7-Methoxy-1,2,3,4-tetrahydro-naphthalen-2-yl)-piperidin-4-yl-propyl-amine | HCID 12135182 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Diisopropylethylamine | HCID 81531 | — |
| Product | HCID 10216398 | HCID 10216398 | — |
Reaction Steps
To a solution of (7-methoxy-1,2,3,4-tetrahydro-naphthalen-2-yl)-piperidin-4-yl-propyl-amine (200 μL of 0.025 M in dichloromethane, 50 μmole) was added 200 μL of 0.25 M solution of morpholine 4-carbonyl chloride in dichloromethane and 30 μL of DIEA. The solution was allowed to stir for 24 h at 25° C. under N2. 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-methoxy-1,2,3,4-tetrahydro-naphthalen-2-yl)-propyl-amino]-piperidin-1-yl}-morpholin-4-yl-methanone 1 (11.9 mg), [M+H]+=461.
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-ad3cc854d19645fcb031ffaf8f373e3a |
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| Source note | uspto-grants-2004_10 |
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