HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 586458Generated: October 29, 2026
HCID 11215611, compound → HCID 11374140, compound
https://huagongshe.com/reaction/586458
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 11215611 | HCID 11215611 | — |
| Reactant | Chloroform methanol | HCID 21584188 | — |
| Product | HCID 11374140 | HCID 11374140 | 100% |
Reaction Steps
4-[6-(6-tert-Butoxycarbonylamino-8-cyclopentyl-7-oxo-7,8-dihydro-pyrido[2,3-d]pyrimidin-2-ylamino)-pyridin-3-yl]-piperazine-1-carboxylic acid tert-butyl ester (0.31 g, 0.511 mmol) prepared as in Example 10, was added to 1:1 chloroform/methanol (20 ml) and the mixture was purged with anhydrous hydrogen chloride gas then stirred at room temperature for 18 hours. The resulting solid was collected by filtration, washed with diethyl ether, and dried in vacuo to provide 6-amino-8-cyclopentyl-2-(5-piperazin-1-yl-pyridin-2-ylamino)-8H-pyrido[2,3-d]pyrimidin-7-one hydrochloride as a yellow solid (0.202 g, 100%). MS (APCI); M++1: Calc'd, 407.48. Found, 407.4. Analyses for C21H26N8O.1.25 H2O.2HCl: Calc'd: C, 50.46; H, 6.02; N, 22.14; Cl (ionic), 15.98; H2O, 4.58. Found: C, 50.25; H, 6.13; N, 22.32; Cl (ionic), 14.13; H2O, 4.49.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06936612B2 |
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| Source dataset | uspto-grants-2005_08 |
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| ORD ID | ord-944c400c1b4445ecb3195ab6fb265b15 |
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| Source note | uspto-grants-2005_08 |
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