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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1967620Generated: October 30, 2026

Diazald → HCID 53380261, compound

https://huagongshe.com/reaction/1967620

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiazaldHCID 6628—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 21225595HCID 21225595—
ReactantHCID 67386574HCID 67386574—
SolventMethanolHCID 887—
ProductHCID 53380261HCID 53380261—

Reaction Steps

The compound was synthesized starting from KOH (15 eq in water), diazald (8 eq), ethylene glycol/Et2O (1/2 v/v, 30 ml), 1-(1H-Benzo[d]imidazol-6-yl)-3-hydroxy-4-methyl-5-(4-morpholinophenyl)-1H-pyrrol-2(5H)-one (0.500 g, 1.28 mmol, 1 eq) and MeOH (10 ml), the product was purified by prep TLC using 4% methanol in chloroform as eluent; yield: 0.100 g (19.34%); MS m/z: 405.1 [M+H]+; 1H-NMR: (400 MHz, DMSO-D6) δ: 12.37 (s, 1H), 8.13 (d, 1H), 7.68-7.64 (m, 1H), 7.50-7.48 (m, 1H), 7.38 (m, 1H), 7.25-7.22 (m, 1H), 7.08-7.06 (m, 2H), 6.82-6.80 (m, 2H), 5.68 (d, 1H), 3.93 (s, 3H), 3.66-3.63 (m, 4H), 3.17-3.01 (m, 4H), 1.66 (s, 3H); HPLC (METHOD [A]): rt 9.33 min (96.37%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420828B2
Source datasetuspto-grants-2013_04
ORD IDord-eb9e1ff140b248d79802ee6e1e862eb8
Source noteuspto-grants-2013_04