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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 564221Generated: October 25, 2026

1,1'-Carbonyldiimidazole → (r)-Tert-butyl 2-(5-(4-carbamoyl-1h-benzimidazol-2-yl)thiophen-2-yl)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/564221

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant2,3-Diaminobenzamide dihydrochlorideHCID 53422807—
Reactant(r)-2-(5-Carboxythiophen-2-yl)pyrrolidine-1-carboxylic acid tert-butyl esterHCID 66759425—
SolventPyridineHCID 1049—
SolventDimethylformamideHCID 6228—
Product(r)-Tert-butyl 2-(5-(4-carbamoyl-1h-benzimidazol-2-yl)thiophen-2-yl)pyrrolidine-1-carboxylateHCID 66760174—

Reaction Conditions

Temperature40 °C

Reaction Steps

To a solution of EXAMPLE 16B (2.4 g) in pyridine (20 mL) and DMF (20 mL) was added CDI (1.6 g), and the mixture was stirred at 40° C. for 1 hour. 2,3-Diaminobenzamide dihydrochloride (1.8 g) was added, and the mixture stirred at ambient temperature overnight and concentrated. The concentrate was stirred in of acetic acid (20 mL) at 80° C. for 4 hours and concentrated. The concentrate was partitioned between ethyl acetate and saturated sodium bicarbonate solution, and the extract was washed with water and concentrated. The concentrate was purified by flash chromatography on silica gel with 40-80% ethyl acetate in hexane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08067613B2
Source datasetuspto-grants-2011_11
ORD IDord-dca1c0030b2c457ebd754654f2b7a5dc
Source noteuspto-grants-2011_11