Hydrochloric Acid → HCID 69211596, compound
Reaction equation
[CH:1]1([NH:8][C:9]2[N:14]=[C:13]([NH:15][CH2:16][CH:17]3[CH2:21][CH2:20][CH2:19][N:18]3[CH2:22][CH3:23])[N:12]=[C:11]([NH:24][C:25]3[CH:30]=[CH:29][C:28]([O:31][CH3:32])=[C:27]([F:33])[CH:26]=3)[N:10]=2)[CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[ClH:34]>CO>[ClH:34].[CH:1]1([NH:8][C:9]2[N:14]=[C:13]([NH:15][CH2:16][CH:17]3[CH2:21][CH2:20][CH2:19][N:18]3[CH2:22][CH3:23])[N:12]=[C:11]([NH:24][C:25]3[CH:30]=[CH:29][C:28]([O:31][CH3:32])=[C:27]([F:33])[CH:26]=3)[N:10]=2)[CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To 130 (2.285g, 5 mmol) in dry methanol (10 mL) was added HCl (5 mL, 5 mmol, 1 M in diethyl ether) and stirred at room temperature for about 1 hour. The reaction was evaporated in vacuo, dissolved in water, filtered, evaporated and then dried under vacuum overnight to afford a solid 164 (2.396 g, 97%), mp 131–133° C.; HPLC: Inertsil ODS-3V C18, 40:30:30 [KH2PO4 (0.01 M, pH 3.2):CH3OH: CH3CN], 264 nm, Rt 7.9 min, 98.2% purity.
Workup
- customThe reaction was evaporated in vacuo
- dissolutiondissolved in water
- filtrationfiltered
- customevaporated
- customdried under vacuum overnight
Sources & evidence
- ORD record
- ord-3291ed4c5169414383ae3c25f1dc3858
- Source dataset
- uspto-grants-2007_01
- Patent number
- US07169785B2
Reaction notes
Loading…