Triethylamine → HCID 72720983, compound
Reaction equation
FC1C=CC=C(F)C=1C[NH2:5].C(N(CC)C(C)C)(C)C.C(N1C=CN=C1)(N1C=CN=C1)=O.C(N(CC)CC)C.[F:39][C:40]1[CH:69]=[C:68](OC)[CH:67]=[C:66]([F:72])[C:41]=1[CH2:42][N:43]1[C:48]2[N:49]=[CH:50][CH:51]=[CH:52][C:47]=2[S:46](=[O:54])(=[O:53])[N:45]([C:55]2[CH:60]=[CH:59][C:58]([O:61][CH3:62])=[C:57]([O:63][CH3:64])C=2)[C:44]1=[O:65]>CN(C=O)C>[F:39][C:40]1[CH:69]=[CH:68][CH:67]=[C:66]([F:72])[C:41]=1[CH2:42][N:43]1[C:48]2[N:49]=[CH:50][CH:51]=[CH:52][C:47]=2[S:46](=[O:53])(=[O:54])[N:45]([C:55]2[CH:60]=[CH:59][C:58]([O:61][CH3:62])=[C:57]([O:63][CH3:64])[N:5]=2)[C:44]1=[O:65]Participants
7
Reactant 5
Product 1
Reagents, catalysts & solvents 1
Procedure
The title compound (57 mg, 0.12 mmol) was prepared in two steps from (IntC3) (165 mg, 0.5 mmol), 2,6-difluorobenzylamine (70 uL, 0.6 mmol) and N,N-diisopropylethylamine (180 uL, 1.0 mmol); followed by 1,1′-carbonyldiimidazole (305 mg, 1.88 mmol), triethylamine (0.13 mL, 0.93 mmol) in DMF (1.5 mL) using the methods of (95).
Sources & evidence
- ORD record
- ord-15b83a24930f4e3aa621a5bde552aeab
- Source dataset
- uspto-grants-2016_02
- Patent number
- US09249160B2
Reaction notes
Loading…