Diisopropylethylamine → N,N-Diethyl-N'-(2-((4-fluorobenzyl)carbamoyl)-3-hydroxy-4-oxo-6,7,8,9-tetrahydro-7,10-ethanopyrimido[1,2-a]azepin-10(4H)-yl)ethanediamide

To a stirred solution of 10-amino-N-(4-fluorobenzyl)-3-hydroxy-4-oxo-4,6,7,8,9,10-hexahydro-7,10-ethanopyrimido[1,2-a]azepine-2-carboxamide (50 mg, 0.122 mmol) in DMF (3 mL) was added 2-(diethylamino)-2-oxoacetic acid (35.5 mg, 0.245 mmol), diisopropyl-ethylamine (0.128 mL, 0.734 mmol), O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (HATU) (93 mg, 0.245 mmol) and 4-(dimethylamino)pyridine (DMAP) (2.99 mg, 0.024 mmol) and the resulting mixture stirred at room temperature for 3 h. After work-up, the crude was then purified by prep HPLC to afford the title compound as a white solid (30 mg, 49% yield). 1H NMR (500 MHz, CDCl3) δ: 12.0 (1 H, brs), 8.7 (1 H, brs), 8.2 (1 H, s), 7.4 (2 H, dd, J=8.09, 5.65 Hz), 7.0 (2 H, t, J=8.55 Hz), 4.6 (2 H, d, J=6.41 Hz), 4.2 (2 H, d, J=3.66 Hz), 3.6 (2 H, q, J=6.82 Hz), 3.3 (2 H, q, J=7.02 Hz), 2.5-2.6 (3 H, m), 2.0-2.1 (2 H, m), 1.9-2.0 (2 H, m), 1.7-1.7 (2 H, m), 1.2 (3 H, t, J=7.02 Hz), 1.1 (3 H, t, J=7.02 Hz). LCMS (M+H)=500.45. HPLC purity: >95%.

1. customAfter work-up, the crude was then purified by prep HPLC

ORDレコード

ord-82365986a80f49c48aa12d661c4088e6

出典データセット

uspto-grants-2012_03

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US08129398B2