Hydrochloric Acid → HCID 67275342, compound
Reaction equation
C([O:3][C:4]([C:6]1[C:15](=[O:16])[C:14]2[C:9](=[N:10][C:11]([N:18]3[CH2:22][CH:21]([OH:23])[CH:20]([NH2:24])[CH2:19]3)=[C:12]([F:17])[CH:13]=2)[N:8](CCC#N)[CH:7]=1)=[O:5])C.[OH-].[Na+].Cl>C(O)C>[NH2:24][C@H:20]1[C@@H:21]([OH:23])[CH2:22][N:18]([C:11]2[N:10]=[C:9]3[C:14]([C:15](=[O:16])[C:6]([C:4]([OH:5])=[O:3])=[CH:7][NH:8]3)=[CH:13][C:12]=2[F:17])[CH2:19]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 50 °C
Procedure
A solution of EXAMPLE 228A (0.1 g) in ethanol (1 mL) at 25° C. was treated with 1N NaOH (1 mL), stirred for 18 hours at 50° C., cooled to 25° C., neutralized using 10% HCl, and filtered. NMR (300 MHz, DMSO-d6) δ ppm 3.7-4.5 (m, 6H), 8.0 (d, 1H), 8.42 (bs, 1H), 8.49 (d, 2H), 13.41 (m, 1H).
Workup
- temperaturecooled to 25° C.
- filtrationfiltered
Sources & evidence
- ORD record
- ord-3da8abae6c8a41d4b46acab68d5e695e
- Source dataset
- uspto-grants-2012_04
- Patent number
- US08163769B2
Reaction notes
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