Hydrochloric Acid → HCID 21834621, compound
Reaction equation
[C:1]([C:3]1[CH:39]=[CH:38][C:6]([CH2:7][N:8]2[C:12]([CH2:13][C:14]([NH:16][CH:17]([CH2:29][NH:30]C(OC(C)(C)C)=O)[C:18]([N:20]([CH3:28])[CH2:21][C:22]3[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=3)=[O:19])=[O:15])=[CH:11][N:10]=[CH:9]2)=[CH:5][CH:4]=1)#[N:2].Cl>CCOC(C)=O>[C:1]([C:3]1[CH:4]=[CH:5][C:6]([CH2:7][N:8]2[C:12]([CH2:13][C:14]([NH:16][CH:17]([CH2:29][NH2:30])[C:18]([N:20]([CH3:28])[CH2:21][C:22]3[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=3)=[O:19])=[O:15])=[CH:11][N:10]=[CH:9]2)=[CH:38][CH:39]=1)#[N:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of the product from Example 27 (86.3 mg, 0.163 mmol) in EtOAc (5 ml) at 0° C. was saturated with gaseous HCl and stirred for 15 min. The solvent was evaporated and the title compound was dried in vacuo.
Workup
- customat 0° C.
- customThe solvent was evaporated
- dry with materialthe title compound was dried in vacuo
Sources & evidence
- ORD record
- ord-33ed2c12b5c043f9b2cb8e25cbdf8611
- Source dataset
- uspto-grants-1998_05
- Patent number
- US05756528
Reaction notes
Loading…