Hydrochloric Acid → HCID 20083125, compound
Reaction equation
[F:1][C:2]1[C:3]([C:21]2[CH2:26][CH2:25][CH2:24][C:23](=[O:27])[CH:22]=2)=[C:4]2[C:9]3=[C:10]([C:12](=[O:19])[C:13]([C:15]([O:17]C)=[O:16])=[CH:14][N:8]3[N:7]([CH3:20])[CH2:6][CH2:5]2)[CH:11]=1.O1CCCC1.Cl>O>[F:1][C:2]1[C:3]([C:21]2[CH2:26][CH2:25][CH2:24][C:23](=[O:27])[CH:22]=2)=[C:4]2[C:9]3=[C:10]([C:12](=[O:19])[C:13]([C:15]([OH:17])=[O:16])=[CH:14][N:8]3[N:7]([CH3:20])[CH2:6][CH2:5]2)[CH:11]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
120 mg of the compound (171) obtained in Example 48 was added to a mixture solution of 3 ml of tetrahydrofuran, 1 ml of 6N hydrochloric acid and 1 ml of water, and the solution was stirred for four days at room temperature. The deposited solid matter was filtered off and washed with water and ethanol in this order to obtain 44 mg of the subject compound (172).
Workup
- filtrationThe deposited solid matter was filtered off
- washwashed with water and ethanol in this order
Sources & evidence
- ORD record
- ord-1006e9c0f0f6454ab6a781ad8c63e829
- Source dataset
- uspto-grants-1995_03
- Patent number
- US05399553
Reaction notes
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