Diisopropylethylamine → HCID 22507691, compound
Reaction equation
[O:1]1[CH2:6][CH2:5][CH:4]([O:7][CH2:8][C:9]2[CH:10]=[C:11]([CH:15]=[CH:16][N:17]=2)[C:12]([OH:14])=O)[CH2:3][CH2:2]1.CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.C(N(C(C)C)C(C)C)C.[O:51]1[CH2:56][CH2:55][O:54][CH2:53][CH:52]1[C:57]1[C:65]2[S:64][C:63]([NH2:66])=[N:62][C:61]=2[C:60]([O:67][CH3:68])=[CH:59][CH:58]=1>C1COCC1.C(Cl)(Cl)Cl>[O:51]1[CH2:56][CH2:55][O:54][CH2:53][CH:52]1[C:57]1[C:65]2[S:64][C:63]([NH:66][C:12](=[O:14])[C:11]3[CH:15]=[CH:16][N:17]=[C:9]([CH2:8][O:7][CH:4]4[CH2:3][CH2:2][O:1][CH2:6][CH2:5]4)[CH:10]=3)=[N:62][C:61]=2[C:60]([O:67][CH3:68])=[CH:59][CH:58]=1Participants
7
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Procedure
From 2-(tetrahydro-pyran-4-yloxymethyl)-isonicotinic acid, HATU and N-ethyldiisopropylamine in THF, then treatment with (+)-7-[1,4]dioxan-2-yl-4-methoxy-benzothiazol-2-ylamine. [α]D20=+84.9° (c=1.05, CHCl3), ES-MS m/e (%): 486 (M+H+, 100).
Sources & evidence
- ORD record
- ord-a8c04aec6a1947ae9cc12110af5d6ca4
- Source dataset
- uspto-grants-2005_03
- Patent number
- US06872833B2
Reaction notes
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