{3-[(acetyloxy)methyl]-2-{4,4-dimethyl-9-oxo-1,10-diazatricyclo[6.4.0.02,6]dodeca-2(6),7-dien-10-yl}pyridin-4-yl}boronic acid

CC(=O)OCc1c(-c2cc(NC(=O)C3CCC3)c(=O)n(C)c2)ccnc1N1CCn2c(cc3c2CC(C)(C)C3)C1=O
Reaction #607479
101b
Yield 56.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
CC(=O)OCc1c(-c2cc(Nc3cnccn3)c(=O)n(C)c2)ccnc1N1CCn2c(cc3c2CC(C)(C)C3)C1=O
Reaction #679963
188a
Yield 40.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
CC(=O)OCc1c(-c2cc(Nc3ccn4ccnc4n3)c(=O)n(C)c2)ccnc1N1CCn2c(cc3c2CC(C)(C)C3)C1=O
Reaction #680027
199f
Yield 40.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
CC(=O)OCc1c(-c2cn(C)c(=O)c(Nc3ccc4nccn4c3)n2)ccnc1N1CCn2c(cc3c2CC(C)(C)C3)C1=O
Reaction #680036
201b
Yield 34.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
CC(=O)OCc1c(-c2cc(Nc3nc4c(s3)CN(C)CC4)c(=O)n(C)c2)ccnc1N1CCn2c(cc3c2CC(C)(C)C3)C1=O
Reaction #680040
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
CC(=O)OCc1c(-c2cc(Nc3ccc(OC4CN(C)C4)cn3)c(=O)n(C)c2)ccnc1N1CCn2c(cc3c2CC(C)(C)C3)C1=O
Reaction #680056
207a
Yield 45.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
CC(=O)OCc1c(-c2cc(Nc3cc4n(n3)CCN(C(C)=O)C4)c(=O)n(C)c2)ccnc1N1CCn2c(cc3c2CC(C)(C)C3)C1=O
Reaction #680069
212a
Yield 56.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
CC(=O)OCc1c(-c2cc(Br)c(=O)n(C)c2)ccnc1N1CCn2c(cc3c2CC(C)(C)C3)C1=O
Reaction #680075
214c
Yield 22.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
CC(=O)OCc1c(-c2cc(Nc3cc(C)n(C)n3)c(=O)n(C)c2)ccnc1N1CCn2c(cc3c2CC(C)(C)C3)C1=O
Reaction #680083
218b
Yield 42.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
CC(=O)OCc1c(-c2cn(C)c(=O)c(Nc3cccc(N)c3)n2)ccnc1N1CCn2c(cc3c2CC(C)(C)C3)C1=O
Reaction #680085
219b
Yield 38.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
CC(=O)OCc1c(-c2cc(Nc3cccc(N)n3)c(=O)n(C)c2)ccnc1N1CCn2c(cc3c2CC(C)(C)C3)C1=O
Reaction #680090
221b
Yield 31.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
COc1ncc(-c2ccnc(N3CCn4c(cc5c4CC(C)(C)C5)C3=O)c2COC(C)=O)cc1Nc1ccnc(C)n1
Reaction #680092
222b
Yield 25.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
CC(=O)OCc1c(-c2cc(Nc3ccc(N4CCN(C5COC5)C[C@@H]4C)cn3)c(=O)n(C)n2)ccnc1N1CCn2c(cc3c2CC(C)(C)C3)C1=O
Reaction #680099
224d
Yield 51.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
CC(=O)OCc1c(-c2cc(Nc3ccnc(C)n3)c(=O)n(C)n2)ccnc1N1CCn2c(cc3c2CC(C)(C)C3)C1=O
Reaction #680101
225b
Yield 47.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
CC(=O)OCc1c(-c2cc(Nc3ccc(C(=O)N4CCOCC4)cn3)c(=O)n(C)n2)ccnc1N1CCn2c(cc3c2CC(C)(C)C3)C1=O
Reaction #680103
226b
Yield 23.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
CCc1nccc(Nc2cc(-c3ccnc(N4CCn5c(cc6c5CC(C)(C)C6)C4=O)c3COC(C)=O)cn(C)c2=O)n1
Reaction #680110
229c
Yield 55.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
CC(=O)OCc1c(-c2cc(Nc3nc4c(s3)CN(C(=O)OC(C)(C)C)CC4)c(=O)n(C)c2)ccnc1N1CCn2c(cc3c2CC(C)(C)C3)C1=O
Reaction #680131
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
CC(=O)OCc1c(-c2cc(Nc3cnc(N4CCN(C5COC5)C[C@@H]4C)cn3)c(=O)n(C)c2)ccnc1N1CCn2c(cc3c2CC(C)(C)C3)C1=O
Reaction #680133
235a
Yield 31.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
CC(=O)OCc1c(-c2cc(Nc3ccc(C4CCN(C)CC4)cn3)c(=O)n(C)c2)ccnc1N1CCn2c(cc3c2CC(C)(C)C3)C1=O
Reaction #680134
236a
Yield 57.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
CC(=O)OCc1c(-c2cc(Nc3ccc(C(=O)N4CCOC[C@H]4C)cn3)c(=O)n(C)n2)ccnc1N1CCn2c(cc3c2CC(C)(C)C3)C1=O
Reaction #680171
248c
Yield 37.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
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