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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 844488Generated: October 29, 2026

Diisopropylethylamine → HCID 18735046, compound

https://huagongshe.com/reaction/844488

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
ReactantHCID 22037061HCID 22037061—
ReactantHCID 22037065HCID 22037065—
SolventDimethylformamideHCID 6228—
ProductHCID 18735046HCID 18735046179.6%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06380224B1
Source datasetuspto-grants-2002_04
ORD IDord-26f870adfb5641ec858b1768aca56c36
Source noteuspto-grants-2002_04