HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2196707Generated: October 29, 2026
HCID 66887603, compound → HCID 67155644, compound
https://huagongshe.com/reaction/2196707
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 66887603 | HCID 66887603 | — |
| Reactant | HCID 67155715 | HCID 67155715 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 67155644 | HCID 67155644 | 30% |
| Product | HCID 67155715 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08338452B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-1ed676054d1049ed9ad903685624d4ee |
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| Source note | uspto-grants-2012_12 |
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