Trifluoroacetic acid → HCID 71553475, compound
Reaction equation
[CH2:1]([N:8]1[CH:12]=[C:11]([C:13]2[C:14]([C:43]([O:45]C(C)(C)C)=[O:44])=[N:15][C:16]([N:19]3[CH2:28][CH2:27][C:26]4[C:21](=[C:22]([C:29](=[O:42])[NH:30][C:31]5[S:32][C:33]6[CH:39]=[C:38]([F:40])[C:37]([F:41])=[CH:36][C:34]=6[N:35]=5)[CH:23]=[CH:24][CH:25]=4)[CH2:20]3)=[CH:17][CH:18]=2)[CH:10]=[N:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(O)(C(F)(F)F)=O>ClCCl>[CH2:1]([N:8]1[CH:12]=[C:11]([C:13]2[C:14]([C:43]([OH:45])=[O:44])=[N:15][C:16]([N:19]3[CH2:28][CH2:27][C:26]4[C:21](=[C:22]([C:29](=[O:42])[NH:30][C:31]5[S:32][C:33]6[CH:39]=[C:38]([F:40])[C:37]([F:41])=[CH:36][C:34]=6[N:35]=5)[CH:23]=[CH:24][CH:25]=4)[CH2:20]3)=[CH:17][CH:18]=2)[CH:10]=[N:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of EXAMPLE 7D (0.085 g) in dichloromethane (0.5 mL) was added TFA (0.5 mL) and the reaction was stirred overnight. The reaction mixture was concentrated and dried to provide the title compound. 1H NMR (300 MHz, dimethylsulfoxide-d6) δ ppm 12.98 (s, 1H), 8.20 (dd, 1H), 7.93-7.83 (m, 2H), 7.70 (d, 1H), 7.58 (dd, 2H), 7.47-7.19 (m, 7H), 6.94 (d, 1H), 5.32 (s, 2H), 4.93 (s, 2H), 3.86 (t, 2H), 2.99 (t, 2H).
Workup
- concentrationThe reaction mixture was concentrated
- customdried
Sources & evidence
- ORD record
- ord-c6089ae74a8345f6aa023ea32f8c12a7
- Source dataset
- uspto-grants-2015_01
- Patent number
- US08940737B2
Reaction notes
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