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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1184364Generated: November 3, 2026

1,1'-Carbonyldiimidazole → HCID 68106726, compound

https://huagongshe.com/reaction/1184364

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantN,N-DimethylsulfamideHCID 134472—
ReactantHCID 68106800HCID 68106800—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68106726HCID 6810672660.3%

Reaction Conditions

Temperature60 °C

Reaction Steps

2-{[(3,5-Dimethoxy-4-methylbenzoyl)(3-phenylpropyl)amino]methyl}-5-methyl-1,3-thiazole-4-carboxylic acid (150 mg) and CDI (78 mg) was added to anhydrous THF (5 mL), followed by heating at 60° C. for about 1 hour. To the reaction mixture were added N,N-dimethylsulfamide (60 mg) and DBU (73 mg) under ice-cooling, respectively, followed by stirring at room temperature overnight. The reaction mixture was concentrated under reduced pressure, and neutralized by the addition of an appropriate amount of purified water and 1 M hydrochloric acid, and then extracted from chloroform. The obtained organic layer was dried over MgSO4, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate=1:2) to obtain 2-{[(3,5-dimethoxy-4-methylbenzoyl)(3-phenylpropyl)amino]methyl}-N-[(dimethylamino)sulfonyl]-5-methyl-1,3-thiazole-4-carboxamide (111 mg) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08669246B2
Source datasetuspto-grants-2014_03
ORD IDord-76794016a20b4c6c9420131cd7a4816d
Source noteuspto-grants-2014_03