[Br:1][C:2]1[CH:28]=[CH:27][C:5]2[N:6]([C:14]([C:16]3[CH:17]=[CH:18][C:19]4[O:24][CH2:23][C:22](=[O:25])[NH:21][C:20]=4[CH:26]=3)=[O:15])[C@@H:7]([CH2:10][C:11]([OH:13])=O)[CH2:8][O:9][C:4]=2[CH:3]=1.C1C[N:32]([P+](ON2N=NC3C=CC=CC2=3)(N2CCCC2)N2CCCC2)CC1.F[P-](F)(F)(F)(F)F.[NH4+].[Cl-].CCOC(C)=O>C(Cl)Cl>[Br:1][C:2]1[CH:28]=[CH:27][C:5]2[N:6]([C:14]([C:16]3[CH:17]=[CH:18][C:19]4[O:24][CH2:23][C:22](=[O:25])[NH:21][C:20]=4[CH:26]=3)=[O:15])[C@@H:7]([CH2:10][C:11]([NH2:32])=[O:13])[CH2:8][O:9][C:4]=2[CH:3]=1{(3S)-7-Bromo-4-[(3-oxo-3,4-dihydro-2H-1,4-benzoxazin-6-yl)carbonyl]-3,4-dihydro-2H-1,4-benzoxazin-3-yl}acetic acid (Intermediate 29a, 160 mg, 0.36 mmol) was dissolved in DCM (3 mL). PyBOP (223 mg, 0.43 mmol) and TEA (0.248 mL, 1.79 mmol) was added followed by NH4Cl (77 mg, 1.43 mmol). The mixture was stirred at rt over weekend. EtOAc (40 mL) was added. Washed with sat. aq. Na2CO3 (2×30 mL), HCl (0.5M, 20 mL) and brine (20 mL). Dried through a phase separator and evaporated under reduced pressure. The residue was purified using a SFC2-MS system and eluting with MeOH on a Waters Viridis 2-EP column 5μ30×250 mm. Pooling of homogenous fraction and removal of solvents in vacuo gave the title compound (46.1 mg, 28.9%).
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