HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 272449Generated: October 27, 2026
2-Aminopyridine → 6-Bromo-8-cyclopentyl-5-methyl-2-(pyridin-2-ylamino)-8H-pyrido[2,3-d]pyrimidin-7-one
https://huagongshe.com/reaction/272449
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Aminopyridine | HCID 10439 | — |
| Reactant | 6-bromo-8-cyclopentyl-5-methyl-2-(methylsulfinyl)pyrido[2,3-d]pyrimidin-7(8H)-one | HCID 11372127 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 6-Bromo-8-cyclopentyl-5-methyl-2-(pyridin-2-ylamino)-8H-pyrido[2,3-d]pyrimidin-7-one | HCID 5330283 | 30% |
Reaction Steps
A mixture of 6-bromo-8-cyclopentyl-2-methanesulfinyl-5-methyl-8H-pyrido[2,3-d]pyrimidin-7-one (370 mg, 1 mmol, prepared as in Example 6 of WO 01/707041 which is incorporated here by reference) and 2-aminopyridine (140 mg, 1.5 mmol) in toluene (5 mL) was heated at 110° C. for 18 hours then cooled to room temperature. The solid formed was collected by filtration and washed with toluene, then acetone, and dried in vacuo to give 6-bromo-8-cyclopentyl-5-methyl-2-(pyridin-2-ylamino)-8H-pyrido[2,3-d]pyrimidin-7-one as a beige solid (22 mg, 30%). mp 267˜268° C. Anal. Calc'd. for C18H18BrN5O.0.33H2O: C, 53.22; H, 4.63; N, 17.24. Found: C, 52.88; H, 4.38; N, 17.04.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07456168B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-5d416e1681974bd3a1034b6f648bb20b |
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| Source note | uspto-grants-2008_11 |
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