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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1927567Generated: November 3, 2026

1,1'-Carbonyldiimidazole → HCID 69231263, compound

https://huagongshe.com/reaction/1927567

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantCyclopropanesulfonamideHCID 15765418—
ReactantHCID 69233646HCID 69233646—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69231263HCID 6923126346.3%

Reaction Steps

A mixture of 9 (50 mg, 0.104 mmol) and CDI (68 mg, 0.418 mmol) in dry THF (5 mL) was heated at reflux for 2 h under nitrogen. The reaction mixture was cooled to room temperature and cyclopropylsulfonamide (101 mg, 0.836 mmol) was added. Then, DBU (73 mg, 0.481 mmol) was added and the reaction mixture was stirred at room temperature for 1 h, and then heated at 55° C. for 24 h. Solvent was evaporated, and the residue partitioned between AcOEt and acidic water (pH=3). The crude material was purified by column chromatography (AcOEt/CH2Cl2/Petroleum ether, 1:1:1). The residue was crystallized in Et2O, filtered to give the target compound contaminated with the cyclopropylsulfonamide. This material was triturated in 1.5 mL of water, filtered, washed with water and dried overnight in the high vacuum pump to give 28 mg (46%) of the target compound as a white powder: m/z=582 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08183277B2
Source datasetuspto-grants-2012_05
ORD IDord-6c453b1a61b043d8b35ca197126b5474
Source noteuspto-grants-2012_05