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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2196674Generated: November 1, 2026

Potassium Carbonate → HCID 44223673, compound

https://huagongshe.com/reaction/2196674

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 67156075HCID 67156075—
SolventMethanolHCID 887—
ProductHCID 44223673HCID 4422367366%

Reaction Conditions

Temperature60 °C

Reaction Steps

2N K2CO3 (1 mL) was added to a solution of 2,6-difluoro-N-(2-(1-methyl-1H-indol-5-yl)-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridin-5-yl)-3-(propylsulfonamido)benzamide (19 mg, 29 mmol) in MeOH (3 mL), and the mixture was heated to 60° C. for 16 hours. The volatiles were removed under reduced pressure, and the resulting residue was partitioned between EtOAc and water. The layers were separated, and the organic layers were dried (MgSO4), filtered and concentrated. Dichloromethane was added to the residue, and the resulting solid was collected by vacuum filtration giving 2,6-difluoro-N-(2-(1-methyl-1H-indol-5-yl)-1H-pyrrolo[2,3-b]pyridin-5-yl)-3-(propylsulfonamido)benzamide (10 mg, 66%). 1H NMR (400 MHz, DMSO-d6) δ 12.04 (s, 1H), 10.84 (s, 1H), 9.80 (s, 1H), 8.33-8.28 (m, 2H), 8.15 (s, 1H), 7.77-7.73 (m, 1H), 7.57-7.52 (m, 2H), 7.39-7.38 (m, 1H), 7.29-7.25 (m, 1H), 6.86 (s, 1H), 6.50-6.49 (m, 1H), 3.83 (s, 3H), 3.15-3.11 (m, 2H), 1.83-1.73 (m, 2H), 1.03-0.98 (m, 3H); m/z (APCI-neg) M−1=522.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338452B2
Source datasetuspto-grants-2012_12
ORD IDord-9ef8310c20994c05a0f384226878aca5
Source noteuspto-grants-2012_12