HCID 67275458, compound → HCID 11778294, compound
Reaction equation
C(OC([NH:8][CH:9]1[CH2:12][N:11]([C:13]2[N:22]=[C:21]3[C:16]([C:17](=[O:30])[C:18]([C:27]([OH:29])=[O:28])=[CH:19][N:20]3CCC#N)=[CH:15][C:14]=2[F:31])[CH2:10]1)=O)(C)(C)C>FC(F)(F)C(O)=O>[NH2:8][CH:9]1[CH2:12][N:11]([C:13]2[N:22]=[C:21]3[C:16]([C:17](=[O:30])[C:18]([C:27]([OH:29])=[O:28])=[CH:19][NH:20]3)=[CH:15][C:14]=2[F:31])[CH2:10]1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of EXAMPLE 20B (0.12 g) in trifluoroacetic acid (6 mL) was stirred for 10 minutes and concentrated; and the concentrate was azeotroped with toluene to provide the desired product. NMR (300 MHz, DMSO-d6) δ 8.51 (s, 1H), 8.03 (m, 1H), 4.58 (m, 2H), 4.26 (m, 2H), 4.16 (br s, 1H).
Workup
- concentrationconcentrated
- customand the concentrate was azeotroped with toluene
Sources & evidence
- ORD record
- ord-df12ccf179c7402eac30d671a06477e2
- Source dataset
- uspto-grants-2012_04
- Patent number
- US08163769B2
Reaction notes
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