HCID 86711369, compound → HCID 86711371, compound

HRID 532924Notes

Reaction equation

HRID 532924 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

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

  1. additionwas added
  2. filtrationThe beige precipitate was filtered off
  3. washwashed with a small amount of diethyl ether (2×)
  4. 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

Loading…