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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2103483Generated: October 26, 2026

Methoxyacetyl chloride → N-[2-(2,6-dioxo-3-piperidyl)-1,3-dioxo-isoindolin-4-yl]-2-methoxy-acetamide

https://huagongshe.com/reaction/2103483

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethoxyacetyl chlorideHCID 96623—
ReactantPomalidomideHCID 134780—
SolventTetrahydrofuranHCID 8028—
ProductN-[2-(2,6-dioxo-3-piperidyl)-1,3-dioxo-isoindolin-4-yl]-2-methoxy-acetamideHCID 9902738100%

Reaction Steps

To a suspension of 4-amino-2-(2,6-dioxo(3-piperidyl))isoindoline-1,3-dione (0.55 g, 2.0 mmol) in THF (30 ml) was added 2-methoxyacetyl chloride (0.43 g, 4.0 mmol). The stirred mixture was heated to reflux for 18 hours. The solvent was evaporated in vacuo and the resulting solid was slurried in diethyl ether (20 ml) and filtered to give 0.69 g (100%) of product as an off-white solid: mp 246-248° C.; 1H NMR (DMSO-d6) δ 11.15 (s, 1H), 10.30 (s, 1H), 8.70 (d, J=8.4 Hz, 1H), 7.86 (t, J=7.8 Hz, 1H), 7.63 (d, J=7.3 Hz, 1H), 5.17 (dd, J=5.2 and 12.7 Hz, 1H), 4.11 (s, 2H), 3.49 (s, 3H), 2.98-2.84 (m, 1H), 2.66-2.47 (m, 2H), 2.12-2.07 (m, 1H); 13C NMR (DMSO-d6) δ 172.67, 169.66, 169.02, 168.25, 166.61, 136.48, 135.91, 131.24, 124.35, 118.31, 116.04, 71.40, 59.10, 48.96, 30.91, 21.94; Anal. Calcd. For C16H15N3O6: C, 55.65; H, 4.38; N, 12.17. Found: C, 55.58; H, 4.40; N, 12.08.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576104B2
Source datasetuspto-grants-2009_08
ORD IDord-718cf0dc53f549e4aa013fd602b334bc
Source noteuspto-grants-2009_08