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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 607257Generated: October 29, 2026

HCID 66808370, compound → HCID 60204801, compound

https://huagongshe.com/reaction/607257

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 66808370HCID 66808370—
ReactantN'-(3-Cyano-6-methyl-pyridin-2-yl)-N,N-dimethyl-formamidineHCID 66808573—
ProductHCID 60204801HCID 60204801—

Reaction Steps

The product from Example 149D was reacted with the product from Example 10B using the procedure described in Example 149E substituting the product from Example 10B for the product from Example 36E to provide {4-[4-(4-Bromo-phenylsulfamoyl)-2-(7-methyl-pyrido[2,3-d]pyrimidin-4-ylamino)-phenylsulfanyl]-phenyl}-carbamic acid tert-butyl ester which was deprotected according to the procedure described in Example 149F, followed by silica gel chromatography provided the title compound as a trifluoroacetic acid salt. 1H NMR (300 MHz, DMSO-D6) δ ppm: 2.74 (s, 3H), 6.64 (d, J=8.46 Hz, 2H), 6.89 (d, J=8.09 Hz, 1H), 7.05 (d, J=9.19 Hz, 2H), 7.12 (d, J=8.82 Hz, 2H), 7.44 (d, J=8.82 Hz, 2H), 7.63 (dd, J=7.72, 0.74 Hz, 1H), 7.74 (s, 1H), 7.79 (dd, J=7.72, 1.10 Hz, 1H), 8.70-8.83 (m, 1H), 8.88 (d, J=8.09 Hz, 1H), 10.55 (s, 1H); MS (ESI+) m/z 593/595 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915411B2
Source datasetuspto-grants-2011_03
ORD IDord-4938ec9fc72a4a56b040eff403f8d6f7
Source noteuspto-grants-2011_03