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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1592526Generated: October 25, 2026

1,3-Dihydro-1,3-dioxo-2H-isoindole-2-butanal → 2-[4-(1-Pyridin-2-yl-ethylamino)-butyl]-isoindole-1,3-dione

https://huagongshe.com/reaction/1592526

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Dihydro-1,3-dioxo-2H-isoindole-2-butanalHCID 77150—
Reactant(R)-1-Pyridin-2-yl-ethylamineHCID 1084918—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventDichloromethaneHCID 6344—
Product2-[4-(1-Pyridin-2-yl-ethylamino)-butyl]-isoindole-1,3-dioneHCID 58997113—

Reaction Steps

Using General Procedure B, reaction of (R)-1-pyridin-2-yl-ethylamine (Shin, C-G et al, Bull. Chem. Soc. Jpn. 2002, 75, 1583-1596) in CH2Cl2 and 4-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-butyraldehyde with NaBH(OAc)3 gave 2-[4-(1-pyridin-2-yl-ethylamino)-butyl]-isoindole-1,3-dione as a yellow oil. 1H NMR (CDCl3) δ 1.37 (d, 3H, J=6.0 Hz), 1.51-1.54 (m, 1H), 1.66-1.71 (m, 2H), 2.02-2.03 (m, 2H), 2.41-2.45 (m, 1H), 2.52-2.57 (m, 1H), 3.66 (t, 2H, J=7.5 Hz), 3.81-3.88 (m, 1H), 7.12-7.14 (m, 1H), 7.28-7.30 (m, 1H), 7.63-7.64 (m, 1H), 7.68-7.71 (m, 2H), 7.81-7.84 (m, 2H), 8.53-8.54 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07291631B2
Source datasetuspto-grants-2007_11
ORD IDord-e6a7187d3c434d95aecd8977cc3d8959
Source noteuspto-grants-2007_11