HCID 86711369, compound → HCID 86711371, compound
Reaction equation
C(OC([NH:8][CH2:9][C:10]([N:12]1[CH:21]([CH2:22][C:23]([O-:25])=[O:24])[C:20]2[N:19]=[CH:18][CH:17]=[C:16]([Cl:26])[C:15]=2[CH2:14][CH2:13]1)=[O:11])=O)(C)(C)C.[Na+]>O1CCOCC1.Cl>[Cl-:26].[C:23]([CH2:22][CH:21]1[C:20]2[N:19]=[CH:18][CH:17]=[C:16]([Cl:26])[C:15]=2[CH2:14][CH2:13][N:12]1[C:10](=[O:11])[CH2:9][NH3+:8])([OH:25])=[O:24]Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
94-8. To a stirred suspension of sodium 2-(7-(2-((tert-butoxycarbonyl)amino)acetyl)-4-chloro-5,6,7,8-tetrahydro-1,7-naphthyridin-8-yl)acetate (540 mg, 1.41 mmol) in dioxane (10 mL), 4N HCl in dioxane (1.76 mL, 7.03 mmol) was added and the reaction mixture was stirred at RT for 48 h. The beige precipitate was filtered off washed with a small amount of diethyl ether (2×). The HCl salt was dried under high vacuo overnight to yield the title compound as beige solid (590 mg) containing a residual amount of NaCl. UPLC-MS: MS 284.1 (M+H+); UPLC rt 0.45 min.
Workup
- additionwas added
- filtrationThe beige precipitate was filtered off
- washwashed with a small amount of diethyl ether (2×)
- dry with materialThe HCl salt was dried under high vacuo overnight
Sources & evidence
- ORD record
- ord-580394b584e8478e93dfa97a81b850c4
- Source dataset
- uspto-grants-2014_10
- Patent number
- US08853203B2
Reaction notes
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