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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1711898Generated: November 2, 2026

Succinic anhydride → HCID 59456977, compound

https://huagongshe.com/reaction/1711898

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSuccinic anhydrideHCID 7922—
ReactantHCID 4473613HCID 4473613—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 59456977HCID 5945697776%

Reaction Steps

A solution of 3-(6-aminopyridin-3-yl)-N-methyl-N-(1-methyl-1H-indol-2-ylmethyl)acrylamide (1.40 g, 4.37 mol) and succinic anhydride (520 mg, 5.24 mmol) in 1,4-dioxane (50 mL) was heated to reflux for 5 h. Another portion of succinic anhydride (520 mg, 5.24 mmol) was then added, and the solution was maintained at reflux overnight. The solvent was removed in vacuo. The residue was dissolved in CH2Cl2, and the solution was washed with satd NaHCO3, water and brine, dried over Na2SO4, and concentrated. Purification by column chromatography (silica gel, CH2Cl2/MeOH, 98:2 to 97:3) gave the title compound (1.40 g, 76%) as an off-white solid and as a mixture of amide rotamers: mp 185-187° C.; 1H NMR (300 MHz, DMSO-d6) δ 8.92-8.88 (m, 1H), 8.41-8.32 (m, 1H 7.69-7.64 (m, 1H), 7.52-7.34 (m, 4H), 7.15-7.09 (m, 1H), 7.04-6.99 (m, 1H), 6.44-6.21 (m, 1H), 5.08-4.87 (m, 2H), 3.73-3.70 (m, 3H), 3.14-3.00 (m, 3H), 2.83-2.81 (m, 4H); MS (ESI) m/e 403 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790709B2
Source datasetuspto-grants-2010_09
ORD IDord-e4c70d16f5694396af89623ea5604582
Source noteuspto-grants-2010_09