HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 607257Generated: October 29, 2026
HCID 66808370, compound → HCID 60204801, compound
https://huagongshe.com/reaction/607257
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 66808370 | HCID 66808370 | — |
| Reactant | N'-(3-Cyano-6-methyl-pyridin-2-yl)-N,N-dimethyl-formamidine | HCID 66808573 | — |
| Product | HCID 60204801 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07915411B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-4938ec9fc72a4a56b040eff403f8d6f7 |
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| Source note | uspto-grants-2011_03 |
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