Hydrochloric Acid → HCID 11420633, compound
Reaction equation
C(OC([N:8]1[CH2:13][CH2:12][N:11]([C:14]2[CH:15]=[N:16][C:17]([NH:20][C:21]3[N:22]=[CH:23][C:24]4[CH:30]=[C:29]([CH2:31][CH2:32][O:33][CH2:34][CH3:35])[C:28](=[O:36])[N:27]([CH:37]5[CH2:41][CH2:40][CH2:39][CH2:38]5)[C:25]=4[N:26]=3)=[CH:18][CH:19]=2)[CH2:10][CH2:9]1)=O)(C)(C)C.[ClH:42]>ClCCl.C(OCC)C>[ClH:42].[CH:37]1([N:27]2[C:25]3[N:26]=[C:21]([NH:20][C:17]4[CH:18]=[CH:19][C:14]([N:11]5[CH2:10][CH2:9][NH:8][CH2:13][CH2:12]5)=[CH:15][N:16]=4)[N:22]=[CH:23][C:24]=3[CH:30]=[C:29]([CH2:31][CH2:32][O:33][CH2:34][CH3:35])[C:28]2=[O:36])[CH2:38][CH2:39][CH2:40][CH2:41]1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
4-{6-[8-Cyclopentyl-6-(2-ethoxy-ethyl )-7-oxo-7,8-dihydro-pyrido[2,3-d]pyrimidin-2-ylamino]-pyridin-3-yl}-piperazine-1-carboxylic acid tert-butyl ester (0.325 g, 0.577 mmol) was dissolved in dichloromethane (4 mL). 2 N HCl in diethyl ether (4 mL) was added and the mixture was stirred at room temperature for 18 hours. The solvent was evaporated to give 8-cyclopentyl-6-(2-ethoxy-ethyl)-2-(5-piperazin-1-yl-pyridin-2ylamino)-8H-pyrido[2,3-d]pyrimidin-7-one hydrochloride salt as a yellow solid (0.292 g, 97.7%). MS (APCl) Calc'd for M+H: 449.2. Found: 449.2. Anal. Calc'd for C25H33N7O22.6HCl,0.35H2O: C, 52.26; H, 6.56; N, 16.88. Found: C, 52.01; H, 6.96; N, 16.88.
Workup
- customThe solvent was evaporated
Sources & evidence
- ORD record
- ord-041e86ddac13454493b41cd09ee8c555
- Source dataset
- uspto-grants-2008_11
- Patent number
- US07456168B2
Reaction notes
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