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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 624619Generated: October 27, 2026

Chloropyruvic acid → HCID 178524791, compound

https://huagongshe.com/reaction/624619

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloropyruvic acidHCID 151137—
Reactant4-Bromo-2-fluorobenzimidamide hydrochlorideHCID 53407891—
ReactantHCID 178432629HCID 178432629—
ProductHCID 178524791HCID 178524791—

Reaction Steps

Scheme 11 shows the synthesis of 5-(2-(4-bromo-2-fluorophenyl)-1H-imidazol-4-yl)-1-isopropyl-3-methyl-1H-1,2,4-triazole V from 4-bromo-2-fluorobenzimidamide hydrochloride 12. 3-Chloro-2-oxopropanoic acid and 12 are reacted with base to give 2-(4-bromo-2-fluorophenyl)-1H-imidazole-4-carboxylic acid 30. Alternatively, 3-bromo-2-oxopropanoic acid can be reacted with 12 to give 30. Reaction of 30 with N′-isopropylacetohydrazonamide 6 and coupling reagent HBTU (N,N,N′,N′-tetramethyl-O-(1H-benzotriazol-1-yl)uronium hexafluorophosphate, 0-(Benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate, CAS Ref No. 94790-37-1) in DMF gives intermediate, 2-(4-bromo-2-fluorophenyl)-N-(1-(2-isopropylhydrazinyl)ethylidene)-1H-imidazole-4-carboxamide 31 which need not be isolated and cyclizes upon heating to give V. Alternatively, 5-(2-(4-chloro-2-fluorophenyl)-1H-imidazol-4-yl)-1-isopropyl-3-methyl-1H-1,2,4-triazole 44, the chloro version of V, can be prepared from 4-chloro-2-fluorobenzonitrile 38 (Scheme 15)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09303043B2
Source datasetuspto-grants-2016_04
ORD IDord-24bbcead7c58444e96b3801769d12222
Source noteuspto-grants-2016_04