Cesium carbonate → HCID 67050703, compound
Reaction equation
Br[C:2]1[CH:23]=[CH:22][C:5]2[C:6]3[N:7]([CH:11]=[C:12]([C:14]4[N:18]([CH:19]([CH3:21])[CH3:20])[N:17]=[CH:16][N:15]=4)[N:13]=3)[CH2:8][CH2:9][O:10][C:4]=2[CH:3]=1.Cl.C([O:29][C:30](=[O:34])[C@H:31]([CH3:33])[NH2:32])(C)(C)C.F[B-](F)(F)F.Cl.C(C1NC=C[N+]=1C(C)C)(C)C.C(=O)([O-])[O-].[Cs+].[Cs+]>COCCOC>[CH:19]([N:18]1[C:14]([C:12]2[N:13]=[C:6]3[N:7]([CH2:8][CH2:9][O:10][C:4]4[CH:3]=[C:2]([NH:32][C@@H:31]([CH3:33])[C:30]([OH:34])=[O:29])[CH:23]=[CH:22][C:5]=43)[CH:11]=2)=[N:15][CH:16]=[N:17]1)([CH3:21])[CH3:20]Participants
Reactant 5
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 8-bromo-2-(2-isopropyl-2H-[1,2,4]triazol-3-yl)-4,5-dihydro-6-oxa-1,3a-diaza-benzo[e]azulene 194 (0.72 g, 1.69 mmol), alanine tert-butyl ester hydrochloride (1.52 g, 8.4 mmol), Rh(COD)2.BF4 (0.07 g, 0.18 mmol), diisopropylimidazolium hydrochloride (0.07 g, 0.35 mmol) and cesium carbonate (4.38 g, 13.4 mmol) in DME (7 mL) was heated at 90° C. under an argon atmosphere for 16 h. The reaction mixture was concentrated in vacuo and the resultant residue partitioned between DCM and water. The aqueous phase was acidified with 1M HCl, extracted with 10% methanol in DCM and the combined organic extracts dried (Na2SO4) and concentrated in vacuo to give (S)-2-[2-(2-Isopropyl-2H-[1,2,4]triazol-3-yl)-4,5-dihydro-6-oxa-1,3a-diaza-benzo[e]azulen-8-ylamino]-propionic acid (0.27 g, 33%). LCMS: RT=2.47 min, [M+H]+=383.
Workup
- concentrationThe reaction mixture was concentrated in vacuo
- customthe resultant residue partitioned between DCM and water
- extractionextracted with 10% methanol in DCM
- dry with materialthe combined organic extracts dried (Na2SO4)
- concentrationconcentrated in vacuo
Sources & evidence
- ORD record
- ord-1109308876624b87be8096f23b56989f
- Source dataset
- uspto-grants-2014_07
- Patent number
- US08785626B2
Reaction notes
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