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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1888349Generated: October 31, 2026

1,1'-Carbonyldiimidazole → {2-[4-(2-Butyl-4-chloro-5-formylimidazol-1-ylmethyl)benzenesulfonylamino]-2-oxoethyl}carbamic acid t-butyl ester

https://huagongshe.com/reaction/1888349

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantN-(tert-butoxycarbonyl)glycineHCID 78288—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant4-(2-Butyl-4-chloro-5-formyl-imidazol-1-ylmethyl)benzenesulfonamideHCID 57931403—
SolventTetrahydrofuranHCID 8028—
Product{2-[4-(2-Butyl-4-chloro-5-formylimidazol-1-ylmethyl)benzenesulfonylamino]-2-oxoethyl}carbamic acid t-butyl esterHCID 5793139468.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

N-Boc-glycine (2.8 g, 16 mmol, 1.0 eq) was dissolved into 50 mL THF. CDI (2.6 g, 16 mmol, 1.0 eq) was added, and the mixture heated to 80° C. for 2 hours. The solution was cooled to room temperature and added to a solution of intermediate (2c) (5.7 g, 16 mmol, 1.0 eq) in 100 mL THF followed by DBU (2.4 mL, 16 mmol, 1.0 eq). The mixture was stirred at room temperature overnight. The mixture was then concentrated, redissolved into 100 mL EtOAc, washed with saturated bicarbonate, saturated aqueous NaCl, dried over MgSO4, and evaporated. The residue was chromatographed (10% MeOH:EtOAc with 0.7% NH3) to yield intermediate (2d) (5.6 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501798B2
Source datasetuspto-grants-2013_08
ORD IDord-053b33ef57e6449cbee39ec92eff3574
Source noteuspto-grants-2013_08