HCID 91551587, compound → HCID 10442600, compound
Reaction equation
C(OC([NH:8][C@H:9]([CH2:16][CH2:17][S:18][CH3:19])[CH:10]([OH:15])[C:11]([O:13][CH3:14])=[O:12])=O)(C)(C)C>Cl.O1CCOCC1>[NH2:8][C@H:9]([CH2:16][CH2:17][S:18][CH3:19])[CH:10]([OH:15])[C:11]([O:13][CH3:14])=[O:12]Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
A solution of Example 11C in 4M HCl in dioxane (10 mL) at room temperature was stirred for 4 hours and concentrated to provide the desired product. MS (APCI(+)) m/e 194 (M−H)−; 1H NMR (300 MHz, DMSO-d6) δ 8.09 (br s, 2H), 7.94 (br s, 1H), 6.58 (m, 0.5H), 6.42 (m, 0.5H), 4.48 (m, 0.5H), 4.30 (m, 0.5H), 3.72 (s, 3H), 2.58 (m, 2H), 2.04 (s, 1.5H), 2.02 (s, 1.5H), 1.82 (m, 2H).
Workup
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-ada714623f4749a78c51c94bdbff051b
- Source dataset
- uspto-grants-2006_04
- Patent number
- US07030262B2
Reaction notes
Loading…