HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 605440Generated: October 31, 2026
HCID 66808370, compound → HCID 60204801, compound
https://huagongshe.com/reaction/605440
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 458D was reacted with the product from Example 9B using the procedure described in Example 458E substituting the product from Example 9B for the product from Example 8E 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 458F, 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, 3 H), 6.64 (d, J=8.46 Hz, 2 H), 6.89 (d, J=8.09 Hz, 1 H), 7.05 (d, J=9.19 Hz, 2 H), 7.12 (d, J=8.82 Hz, 2 H), 7.44 (d, J=8.82 Hz, 2 H), 7.63 (dd, J=7.72, 0.74 Hz, 1 H), 7.74 (s, 1 H), 7.79 (dd, J=7.72, 1.10 Hz, 1 H), 8.70-8.83 (m, 1 H), 8.88 (d, J=8.09 Hz, 1 H), 10.55 (s, 1 H); MS (ESI+) m/z 593/595 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07910595B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-d5ec6b291f634d5c966020bd9bfe1b06 |
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| Source note | uspto-grants-2011_03 |
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