Hydrochloric Acid → HCID 59333755, compound
Reaction equation
[OH:1][CH2:2][CH2:3][N:4]([C:35]1[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=1)[C:5]1[C:6]2[CH2:27][N:26](C(OC(C)(C)C)=O)[CH2:25][CH2:24][C:7]=2[N:8]=[C:9]([NH:11][C:12]2[CH:17]=[CH:16][C:15]([C:18]3[CH:19]=[N:20][N:21]([CH3:23])[CH:22]=3)=[CH:14][CH:13]=2)[N:10]=1.Cl>CO>[CH3:23][N:21]1[CH:22]=[C:18]([C:15]2[CH:14]=[CH:13][C:12]([NH:11][C:9]3[N:10]=[C:5]([N:4]([C:35]4[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=4)[CH2:3][CH2:2][OH:1])[C:6]4[CH2:27][NH:26][CH2:25][CH2:24][C:7]=4[N:8]=3)=[CH:17][CH:16]=2)[CH:19]=[N:20]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 70 °C
Procedure
tert-Butyl 4-((2-hydroxyethyl)(phenyl)amino)-2-(4-(1-methyl-1H-pyrazol-4-yl)phenylamino)-7,8-dihydropyrido[4,3-d]pyrimidine-6(5H)-carboxylate (882 mg, 1.63 mmol) was dissolved in methanol (5 mL). Hydrochloric acid (0.136 mL, 1.63 mmol) was added and the reaction mixture was stirred at 70° C. for 1 h. The solvent was evaporated under reduced pressure and the crude was used in the next step without further purification.
Workup
- customThe solvent was evaporated under reduced pressure
- customthe crude was used in the next step without further purification
Sources & evidence
- ORD record
- ord-aa9dc0e83d0c47c1a890503fb7b77013
- Source dataset
- uspto-grants-2012_05
- Patent number
- US08188101B2
Reaction notes
Loading…