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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1694314Generated: November 3, 2026

Diisopropylethylamine → HCID 59486429, compound

https://huagongshe.com/reaction/1694314

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantHOAtHCID 181649—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant(1R)-6-[(Piperidin-1-yl)methyl]-1,2,3,4-tetrahydronaphthalen-1-amineHCID 56594240—
Reactant2-(2-(6-Methoxynaphthalen-2-ylsulfonyl)-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazin-1-yl)acetic acidHCID 59486421—
SolventDichloromethaneHCID 6344—
ProductHCID 59486429HCID 5948642955%

Reaction Steps

DIPEA (2.5 eq.), HOAt (1.0 eq.) and EDCl (1.5 eq.) were added to a solution of 2-(2-(6-methoxynaphthalen-2-ylsulfonyl)-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazin-1-yl)-acetic acid S2 (0.195 mmol, 1.0 eq.) in DCM (3 ml) at 0° C. and the mixture was stirred for 15 min at RT. Then (R)-6-(piperidin-1-ylmethyl)-1,2,3,4-tetrahydro-naphthalen-1-amine A6 (0.234 mmol, 1.2 eq.) in DCM (2 ml) was added at 0° C. and the mixture was stirred overnight at RT. The reaction mixture was diluted with DCM and extracted with aqueous NaHCO3 solution, aqueous NH4Cl solution, water and saturated NaCl solution. The organic phase was dried (Na2SO4), concentrated to small volume and purified by column chromatography (alox). Yield: 55%; m/z=627.4 [MH]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158628B2
Source datasetuspto-grants-2012_04
ORD IDord-4ddd0ebc53af424aae12e33090d26fac
Source noteuspto-grants-2012_04