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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2196707Generated: October 29, 2026

HCID 66887603, compound → HCID 67155644, compound

https://huagongshe.com/reaction/2196707

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 66887603HCID 66887603—
ReactantHCID 67155715HCID 67155715—
SolventMethanolHCID 887—
ProductHCID 67155644HCID 6715564430%
ProductHCID 67155715HCID 67155715—

Reaction Steps

N-(3-Ethoxy-1-tosyl-1H-pyrrolo[2,3-b]pyridin-5-yl)-2,6-difluoro-3-(propylsulfonamido)benzamide was prepared following Example 32, Step D, substituting 3-ethoxy-1-tosyl-1H-pyrrolo[2,3-b]pyridin-5-amine for 3-iodo-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridin-5-amine. N-(3-Ethoxy-1-tosyl-1H-pyrrolo[2,3-b]pyridin-5-yl)-2,6-difluoro-3-(propylsulfonamido)benzamide was then subjected to methanol/aqueous potassium carbonate at 60° C. for 1 hour to give N-(3-ethoxy-1H-pyrrolo[2,3-b]pyridin-5-yl)-2,6-difluoro-3-(propylsulfonamido)benzamide (30%). 1H NMR (400 MHz, d6-DMSO) δ 11.03 (s, 1H), 10.83 (s, 1H), 8.31-8.35 (m, 2H), 7.10-7.54 (m, 2H), 7.05 (s, 1H), 4.00-4.06 (m, 2H), 3.00-3.06 (m, 2H), 1.70-1.76 (m, 2H), 1.36-1.40 (m, 3H), 0.94-1.01 (m, 3H); (APCI-pos) M+1=439.1 (APCI-pos) M+1=439.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338452B2
Source datasetuspto-grants-2012_12
ORD IDord-1ed676054d1049ed9ad903685624d4ee
Source noteuspto-grants-2012_12