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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 911881Generated: November 2, 2026

1,1'-Carbonyldiimidazole → HCID 178518918, compound

https://huagongshe.com/reaction/911881

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant3-(2-(5-Bromo-3-phenoxypyridin-2-ylamino)thiazol-4-yl)propanehydrazideHCID 86631513—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178518918HCID 17851891828.31%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a mixture of 3-(2-(5-bromo-3-phenoxypyridin-2-ylamino)thiazol-4-yl)propanehydrazide (0.150 g, 0.345 mmol) in THF (5 mL) was added TEA (0.04814 mL, 0.3454 mmol) and cooled in an ice bath. To this mixture was added. CDI (0.0672 g, 0.414 mmol) in one portion. The mixture was allowed to warn to ambient temperature and was then heated at 50° C. overnight. The reaction was concentrated to dryness, dissolved in CH2Cl2 and washed with water, dried over Na2SO4, concentrated to a residue that was purified by preparative HPLC to give the title compound (0.045 g, 28.31% yield) was white solids. 1H NMR (d6DMSO) δ 2.91 (s, 4H), 6.75 (s, 1H), 7.10 (d, J=7.8 Hz, 2H), 7.21 (t, J=7.4 Hz, 1H), 7.40 (d, J=2.1 Hz, 1H), 7.44 (t, J=7.9 Hz, 2H), 8.22 (d, J=2.1 Hz, 1H), 11.03 (br s, 1H), 12.04 (br s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022223B2
Source datasetuspto-grants-2011_09
ORD IDord-3bab2147a3a34d1d86ad2f2c02797e6e
Source noteuspto-grants-2011_09