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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 639748Generated: October 30, 2026

1,1'-Carbonyldiimidazole → HCID 16222379, compound

https://huagongshe.com/reaction/639748

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant3,3-Difluorocyclobutane-1-carboxylic acidHCID 13777789—
ReactantN-hydroxy-4-{4-methyl-5-[2-(trifluoromethyl)phenyl]-4H-1,2,4-triazol-3-yl}bicyclo[2.2.2]octane-1-carboximidamideHCID 72262919—
SolventDichloromethaneHCID 6344—
ProductHCID 16222379HCID 16222379—

Reaction Steps

N′-Hydroxy-4-{4-methyl-5-[2-(trifluoromethyl)phenyl]-4H-1,2,4-triazol-3-yl}bicyclo[2.2.2]octane-1-carboximidamide (1-G) (120 mg, 0.305 mmol) was added to a pre-stirred solution of 3,3-difluorocyclobutanecarboxylic acid 2-D (166 mg, 1.22 mmol) and carbonyldiimidazole (198 mg, 1.22 mmol) in CH2Cl2 (8 ml). The resulting mixture was stirred at room temperature for 48 h, then concentrated. The solid was resuspended in toluene and refluxed under nitrogen atmosphere for 3 h. The product was purified by C-18 reverse phase HPLC eluting with 30-80% acetonitrile/water with 0.1% TFA to yield 2-E as a white powder. MS (ESI+)=494.2 (M+1); 1H NMR (500 MHz, CDCl3): δ 2.09 (6H, m), 2.31 (6H, m), 3.03-3.11 (4H, m), 3.57-3.61 (4H, m), 7.56 (1H, m), 7.71 (2H, m), 7.86 (1H, m) ppm. Shh-Light II Assay: IC50: 1.4 μM.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07691887B2
Source datasetuspto-grants-2010_04
ORD IDord-5f1188499bc9499daeb916851c774116
Source noteuspto-grants-2010_04