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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1625455Generated: November 1, 2026

Boronic Acid → HCID 59362384, compound

https://huagongshe.com/reaction/1625455

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoronic AcidHCID 61668—
ReactantFuran-3-boronic acidHCID 2734358—
ReactantHCID 24861061HCID 24861061—
ProductHCID 59362384HCID 59362384—

Reaction Steps

Except where indicated, 1-(3,4-Difluoro-benzyl)-2-oxo-1,2-dihydro-pyridine-3-carboxylic acid 3-(5-furan-3-yl-1H-pyrrolo[2,3-b]pyridin-3-yl)-benzylamide was synthesized as per Example 91, 1-(3,4-Difluoro-benzyl)-2-oxo-1,2-dihydro-pyridine-3-carboxylic acid 3-(5-thiophen-3-yl-1H-pyrrolo[2,3-b]pyridin-3-yl)-benzylamide using Furan-3-boronic acid as boronic acid to yield the product. 1H NMR (500 MHz, DMSO-d6) d ppm 11.973 (s, 1H) 10.118 (t, J=5.7 Hz, 1H) 8.568 (s, 1H) 8.400 (d, J=7.2 Hz, 1H) 8.374 (s, 1H) 8.248 (s, 1H) 8.221 (d, J=6.7 Hz, 1H) 7.863 (d, J=2.6 Hz, 1H) 7.755 (m, 2H) 7.622 (d, J=7.7 Hz, 1H) 7.439-7.308 (m, 3H) 7.198 (d, J=7.7 Hz, 1H) 7.144-7.100 (m, 1H) 7.073 (s, 1H) 6.586 (t, J=6.7 Hz, 1H) 5.168 (s, 2H) 4.593 (d, J=6.2 Hz, 2H); MS m/z=537.36 M+H.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778977B2
Source datasetuspto-grants-2014_07
ORD IDord-0392c51c10d945dd938f5c1cf4f092ef
Source noteuspto-grants-2014_07