Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 268716Generated: November 1, 2026

1,2-Dichloroethane → N-t-Butoxycarbonyl-5-[(morpholin-4-yl)carbonyl]isoindoline

https://huagongshe.com/reaction/268716

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantMorpholineHCID 8083—
ReactantTriethylamineHCID 8471—
Reactant2-(tert-Butoxycarbonyl)-2,3-dihydro-1H-isoindole-5-carboxylic acidHCID 16450143—
CatalystHOAtHCID 181649—
SolventDichloromethaneHCID 6344—
ProductN-t-Butoxycarbonyl-5-[(morpholin-4-yl)carbonyl]isoindolineHCID 17986287—

Reaction Steps

A mixture of N-t-butoxycarbonyl-5-carboxyisoindoline (D13) (300 mg), EDC (440 mg), HOAT (10 mg), triethylamine (0.4 ml) and morpholine (0.12 ml) in DCM (10 ml) was stirred overnight and then evaporated. The residue was redissolved in EtOAc (10 ml), washed with saturated NaHCO3 solution (10 ml), water (10 ml), brine (10 ml), dried (MgSO4) and evaporated. The residue was chromatographed on a silica gel flash column [step gradient 70-90% EtOAc in light petroleum 40-60] to give the title compound (D19) (314 mg). MS electrospray (+ion) 333 (MH+). 1H NMR δ (CDCl3): 7.30 (3H, m), 4.70 (2H, m), 4.67 (2H, m), 3.70 (8H, m), 1.52 (9H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07446103B2
Source datasetuspto-grants-2008_11
ORD IDord-117746c291fb4161a0b17860b2855f4e
Source noteuspto-grants-2008_11