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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033805Generated: November 3, 2026

2-Chlorobenzoic Acid → HCID 19024441, compound

https://huagongshe.com/reaction/1033805

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chlorobenzoic AcidHCID 8374—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 19024447HCID 19024447—
SolventTetrahydrofuranHCID 8028—
ProductHCID 19024441HCID 1902444168%

Reaction Conditions

Temperature55 °C

Reaction Steps

A solution of 21 mg (0.13 mmole) of 2-chlorobenzoic acid and 22 mg (0.13 mmole) of 1,1'-carbonyldiimidazole (CDI) in 0.8 mL of THF was stirred under N2 at 65° C. for 2.5 hours. Subsequently, a solution of 32 mg (0.067 mmole) of 1-[N-pentyl-N-[(2'-sulfamoylbiphenyl-4-yl)methyl]carbamoyl]indoline (from Step B) and 20 μL (0.13 mmole) of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) in 0.8 mL of THF was added. After stirring for 29 hours at 55° C., the mixture was partitioned between EtOAc and 5% citric acid (aqueous). The organic layer was washed with water and brine, then dried over sodium sulfate. After filtration and removal of volatiles, the crude product was flash chromatographed over silica gel (gradient elution with 0.5-1.0% MeOH in CH2Cl2) to give 28 mg (68%) of the title compound as an off-white solid, mp 83°-85° C.; homogeneous by TLC (95:5 MeOH--CH2Cl2); FAB-MS m/e 616 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05312820
Source datasetuspto-grants-1994_05
ORD IDord-2a641906d4de45a2bdbf6204a7317a11
Source noteuspto-grants-1994_05