Hydrochloric Acid → HCID 67227175, compound
Reaction equation
[ClH:1].[CH3:2][O:3][C:4]1[CH:5]=[C:6](/[C:12](=[CH:15]/[C:16]2[CH:17]=[N:18][CH:19]=[CH:20][CH:21]=2)/[C:13]#[N:14])[CH:7]=[CH:8][C:9]=1[O:10][CH3:11]>>[ClH:1].[CH3:2][O:3][C:4]1[CH:5]=[C:6](/[C:12](=[CH:15]/[C:16]2[CH:17]=[N:18][CH:19]=[CH:20][CH:21]=2)/[C:13]#[N:14])[CH:7]=[CH:8][C:9]=1[O:10][CH3:11]Participants
3
Procedure
0.1N Hydrochloric acid (21.0 mL) was added to Compound 34 (500 mg), and purified water (40 mL), acetonitrile (50 mL), and chloroform (1 mL) were added to the mixture, to thereby dissolve the mixture. The solution was stirred in the dark at room temperature for 3 hours, and the solvent was evaporated to dryness. The precipitated crystals were thoroughly dried, to thereby yield the target product (yield: 550 mg, 97%).
Workup
- custompurified water (40 mL), acetonitrile (50 mL), and chloroform (1 mL)
- additionwere added to the mixture
- dissolutionto thereby dissolve the mixture
- customthe solvent was evaporated to dryness
- customThe precipitated crystals were thoroughly dried
Sources & evidence
- ORD record
- ord-d79b3b3e1f7743afa32766d9b555e9b1
- Source dataset
- uspto-grants-2014_04
- Patent number
- US08697742B2
Reaction notes
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