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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1746282Generated: November 1, 2026

N-(Methoxycarbonyl)maleimide → HCID 71230565, compound

https://huagongshe.com/reaction/1746282

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(Methoxycarbonyl)maleimideHCID 580610—
Reactant1418310-93-6HCID 71230589—
SolventSodium BicarbonateHCID 516892—
ProductHCID 71230565HCID 7123056520%

Reaction Conditions

Temperature0 °C

Reaction Steps

To 4-(4-aminobutyl)-1,2,4-triazolidine-3,5-dione hydrochloride (I-14a: 42 mg, 0.201 mmol) in NaHCO3 sat aqueous solution (1.006 mL) at 0° C. was added N-methoxycarbonylmaleimide (31.2 mg, 0.201 mmol). The mixture was stirred at 0° C. for 1 h, and then at room temperature for 2 h. The mixture was purified by preparative hplc (0-60% CH3CN/(0.1% TFA in H2O)), and then lyophilized, giving 4-(4-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)butyl)-1,2,4-triazolidine-3,5-dione (I-14b: 10 mg, 20%) a white solid. LC-MS (M+1) 253.3, t=0.89 minute. 1H NMR (400 MHz, CD3CN) δ ppm 1.51-1.62 (m, 4H) 3.45 (t, J=6.44 Hz, 2H) 3.49 (t, J=6.44 Hz, 2 H) 6.76 (s, 2 H) 7.52 (br. s., 2 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09149541B2
Source datasetuspto-grants-2015_10
ORD IDord-867a0bc41f704415a120b9519ec6bbe4
Source noteuspto-grants-2015_10