HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 844488Generated: October 29, 2026
Diisopropylethylamine → HCID 18735046, compound
https://huagongshe.com/reaction/844488
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 2733084 | — |
| Reactant | HCID 22037061 | HCID 22037061 | — |
| Reactant | HCID 22037065 | HCID 22037065 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 18735046 | HCID 18735046 | 179.6% |
Reaction Steps
1,2,3,4-Tetrahydro-1-(3-pyridinylmethyl)-2-naphthalenamine bis-hydrochloride 4 (0.75 g, 2.41 mmol) was reacted with 2-(4-acetyl-4-phenyl-piperidin-1-yl)acetic acid (0.86 g, 2.65 mmol), N,N-diisopropylethylamine (2.0 mL, 11.3 mmol) and HBTU (1.01 g, 2.65 mmol) in N,N-dimethylformamide (15 mL) at room temperature for 2 h as described above in EXAMPLES 7-8. The product was collected by filtration from the aqueous work-up. This material was dissolved in isopropanol (˜30 mL) and treated with a saturated solution of hydrochloric acid in isopropanol (˜5 mL). The solvent was evaporated in vacuo, and the residue was triturated with diethyl ether to give 4-acetyl-4-phenyl-N-[cis-1,2,3,4-tetrahydro-1-(3-pyridinylmethyl)-2-naphthalenyl]-1-piperidineacetamide bis-hydrochloride 21 as an amorphous pale yellow solid (1.2 g, 90%): MS m/e 482 (MH+) (Scheme 34).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06380224B1 |
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| Source dataset | uspto-grants-2002_04 |
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| ORD ID | ord-26f870adfb5641ec858b1768aca56c36 |
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| Source note | uspto-grants-2002_04 |
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