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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1506813Generated: October 29, 2026

2-Dodecen-1-ylsuccinic anhydride → HCID 68009207, compound

https://huagongshe.com/reaction/1506813

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Dodecen-1-ylsuccinic anhydrideHCID 29772—
ReactantHCID 67531620HCID 67531620—
ReactantHCID 178479113HCID 178479113—
ProductHCID 68009207HCID 6800920791%

Reaction Steps

Following the same procedure to synthesize 1-(2-amino-1H-benzo[d]imidazol-6-yl)-1H-pyrrole-2,5-dione hydrochloride, tert-butyl 6-amino-2-(bis(tert-butoxycarbonyl)amino)-1H-benzo[d]imidazole-1-carboxylate (0.161 g, 0.359 mmol) was reacted with (2-dodecen-1-yl)succinic anhydride (0.096 g, 0.359 mmol) to give the title product (0.142 g, 91% yield) as a yellow solid. 1H NMR (300 MHz, CD3OD) δ 7.46 (d, 1H), 7.28 (s, 1H), 7.19 (d, 1H), δ 5.62 (m, 1H), δ 5.47 (m, 1H), δ 3.19 (t, 1H), δ 2.99 (t, 1H), δ 2.65 (m, 2H), δ 2.06 (m, 2H), δ 1.63 (d, 2H), δ 1.28 (m, 14H), δ 0.89 (t, 3H) ppm; 13C NMR (75 MHz, CD3OD) δ 179.8, 176.9, 151.5, 134.9, 133.7, 129.4, 128.3, 124.9, 122.8, 111.4, 110.6, 40.2, 36.1, 34.9, 33.7, 32.5, 31.9, 29.6, 29.4, 29.1, 27.2, 22.6, 13.4 ppm; HRMS (ESI) Calcd for C23H32N4O2 (M+) 396.2525. Found 396.2522.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221765B2
Source datasetuspto-grants-2015_12
ORD IDord-c1e8aa2880e4449ba3b377305238b7ee
Source noteuspto-grants-2015_12