HCID 67275514, compound → HCID 10244293, compound
Reaction equation
C([N:5]1[C:14]2[C:9](=[CH:10][CH:11]=[C:12]([N:15]3[CH2:19][CH2:18][CH2:17][CH2:16]3)[N:13]=2)[C:8](=[O:20])[C:7]([C:21]([O:23]CC)=[O:22])=[CH:6]1)(C)(C)C>C(O)C.Cl.C(OCC)C>[O:20]=[C:8]1[C:9]2[C:14](=[N:13][C:12]([N:15]3[CH2:16][CH2:17][CH2:18][CH2:19]3)=[CH:11][CH:10]=2)[NH:5][CH:6]=[C:7]1[C:21]([OH:23])=[O:22]Participants
5
Reactant 1
Product 1
Reagents, catalysts & solvents 3
Procedure
A solution of Example 74A (63.2 mg) in ethanol (2.5 mL) and 6M HCl (2.5 mL) was heated in a sealed tube at 130° C. for 18 hours then cooled, diluted with diethyl ether, and filtered. NMR (300 MHz, DMSO-d6) δ 8.43 (s, 1H), 8.22 (m, 1H), 6.80 (m, 1H), 3.55 (m, 4H), 2.00 (m, 4H).
Workup
- temperaturethen cooled
- filtrationfiltered
Sources & evidence
- ORD record
- ord-c5c8c1ade1c942509877e988b62dd997
- Source dataset
- uspto-grants-2012_04
- Patent number
- US08163769B2
Reaction notes
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