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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1497937Generated: October 30, 2026

1,1'-Carbonyldiimidazole → HCID 71280386, compound

https://huagongshe.com/reaction/1497937

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant2,2-Difluorocyclopropane-1-carboxylic acidHCID 2782823—
ReactantN-(5-(N'-hydroxycarbamimidoyl)-2-methylphenyl)imidazo[1,2-a]pyridine-3-carboxamideHCID 86677441—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 71280386HCID 71280386—

Reaction Conditions

Temperature120 °C

Reaction Steps

To a stirring solution of 2,2-difluorocyclopropanecarboxylic acid (325 mg, 2.66 mmol) in anhydrous NMP (7 mL) was added 1,1′-carbonyldiimidazole (CDI) (432 mg, 2.66 mmol). The reaction was stirred for 3 minutes. N-(5-(N′-hydroxycarbamimidoyl)-2-methylphenyl)imidazo[1,2-a]pyridine-3-carboxamide (9) (825 mg, 2.66 mmol) was added and the reaction was stirred for 25 minutes. Then, the reaction was heated at 120° C. for minutes. The crude product was purified on silica gel using 10% MeOH in dichloromethane to give N-(5-(5-(2,2-difluorocyclopropyl)-1,2,4-oxadiazol-3-yl)-2-methylphenyl)imidazo[1,2-a]pyridine-3-carboxamide (F64). 1H NMR (400 MHz, d6-DMSO) δ 9.60 (d, J=7.2 Hz, 1H), 8.56 (d, J=1.6 Hz, 1H), 8.51 (s, 1H), 8.12 (bs, 1H), 7.87 (dd, J=2.0, 7.8 Hz, 1H), 7.82 (d, J=9.2 Hz, 1H), 7.58-7.53 (m, 1H), 7.44 (d, J=8.0 Hz, 1H), 7.16 (td, J=0.8, 6.8 Hz, 1H), 3.19-3.12 (m, 1H), 2.48 (s, 3H), 2.45-2.36 (m, 1H), 2.27-2.18 (m, 1H). MS m/z 396.1 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09199981B2
Source datasetuspto-grants-2015_12
ORD IDord-8a75bf68a57d416c9e65fadc64c95fe8
Source noteuspto-grants-2015_12