Diisopropylethylamine → HCID 68283908, compound
Reaction equation
Cl.[CH2:2]([O:5][C:6]([C@@H:8]1[CH2:13][C@@H:12]2[C@@H:10]([CH2:11]2)[N:9]1[C:14]([OH:16])=O)=[O:7])[CH:3]=[CH2:4].[C:17]([C:20]1[C:28]2[C:23](=[N:24][CH:25]=[CH:26][CH:27]=2)[N:22]([CH2:29]C(O)=O)[N:21]=1)(=[O:19])[CH3:18].CN(C(ON1N=NC2C=CC=CC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.CCN(C(C)C)C(C)C>CN(C=O)C>[CH2:2]([O:5][C:6]([C@@H:8]1[CH2:13][C@@H:12]2[C@@H:10]([CH2:11]2)[N:9]1[C:14](=[O:16])[CH2:29][N:22]1[C:23]2=[N:24][CH:25]=[CH:26][CH:27]=[C:28]2[C:20]([C:17](=[O:19])[CH3:18])=[N:21]1)=[O:7])[CH:3]=[CH2:4]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of (1R,3S,5R)-2-azabicyclo[3.1.0]hexane-2,3-dicarboxylic acid 3-allyl ester hydrochloride (1.03 g, 6.43 mmol), (3-acetyl-pyrazolo[3,4-b]pyridin-1-yl)-acetic acid (prepared as described in Part A, 1.3 g, 5.93 mmol) and HBTU (2.70 g, 7.12 mmol) in DMF (19.7 mL) was added DIPEA (3.11 mL, 17.8 mmol). The reaction mixture was stirred for 16 h at RT. DMF was evaporated. The residue was poured into NH4Cl (sat. aq. solution) and extracted with EtOAc (3×50 mL). The organic layers were combined, dried over Na2SO4, filtered and concentrated. The crude residue was purified by flash column chromatography on silica gel (c-hexane to c-hexane/EtOAc 0:10) to give the title compound. Rf, TLC (EtOAc)=0.6; MS (LCMS): 369.0 [M+H]+, 391.0 [MH+Na]+; tR (HPLC conditions d): 2.78 min.
Workup
- customDMF was evaporated
- additionThe residue was poured into NH4Cl (sat. aq. solution)
- extractionextracted with EtOAc (3×50 mL)
- dry with materialdried over Na2SO4
- filtrationfiltered
- concentrationconcentrated
- customThe crude residue was purified by flash column chromatography on silica gel (c-hexane to c-hexane/EtOAc 0:10)
Sources & evidence
- ORD record
- ord-307bdf1537c84d64a285ba8e3ae475c5
- Source dataset
- uspto-grants-2016_07
- Patent number
- US09388199B2
Reaction notes
Loading…