6-bromo-3,4-dihydro-2H-isoquinolin-1-one

O=C1NCCc2cc(NCc3ccccc3)ccc21
Reaction #341
Ausbeute 0.0%750 AstraZeneca ELN dataset
O=C1NCCc2cc(NCc3ccccc3)ccc21
Reaction #342
Ausbeute 0.0%750 AstraZeneca ELN dataset
O=C1NCCc2cc(NCc3ccccc3)ccc21
Reaction #343
Ausbeute 0.0%750 AstraZeneca ELN dataset
O=C1NCCc2cc(NCc3ccccc3)ccc21
Reaction #344
Ausbeute 0.0%750 AstraZeneca ELN dataset
CC(C)(C)OC(=O)N(c1ccc(N2CCOCC2)cc1)c1ncc(-c2ccc3c(c2)CCNC3=O)n2ncnc12
Reaction #230871
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C1c2ccc(Br)cc2CCN1CCCc1ccccc1
Reaction #239152
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCN1CCc2cc(Br)ccc2C1=O
Reaction #276706
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C1c2ccc(Br)cc2CCN1CCCc1ccccc1
Reaction #344228
2-(3-phenylpropyl)-6-bromo-1-oxo-1,2,3,4-tetrahydroisoquinoline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_11
O=C1NCCc2cc(C3CC3)ccc21
Reaction #397076
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC1(C)OC(=O)N(c2ccc3c(c2)CCNC3=O)[C@H]1c1ccccc1
Reaction #612556
(S)-5,5-dimethyl-3-(1-oxo-1,2,3,4-tetrahydroisoquinolin-6-yl)-4-phenyloxazolidin-2-one
Ausbeute 53.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
—
Reaction #635921
solid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_05
CC(C)(C)OC(=O)N(c1ccc(N2CCOCC2)cc1)c1ncc(-c2ccc3c(c2)CCNC3=O)n2ncnc12
Reaction #693101
compound
Ausbeute 37.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_03
Cc1cnc(NC(=O)c2cc(Oc3ccc4c(c3)CCNC4=O)cc(OC3CCOC3)c2)cn1
Reaction #895640
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
O=C1c2ccc(Br)cc2CCN1Cc1ccc(-c2ccc(F)cc2)cn1
Reaction #1208251
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
Brc1ccc2c(c1)CCNC2
Reaction #1688223
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_11
O=C1c2ccc(Br)cc2CCN1CCCc1ccccc1
Reaction #1828884
2-(3-phenylpropyl)-6-bromo-1-oxo-1,2,3,4-tetrahydroisoquinoline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1994_08
O=C1c2ccc(Br)cc2CCN1Cc1ccc(-c2ccc(F)cc2)cn1
Reaction #1828913
6-bromo-2-{[5-(4-fluorophenyl)-2-pyridyl]methyl}-1-oxo-1,2,3,4 -tetrahydroisoquinoline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1994_08
CC(C)(C)OC(=O)N(c1ccc(N2CCOCC2)cc1)c1ncc(-c2ccc3c(c2)CCNC3=O)n2ncnc12
Reaction #1871120
compound
Ausbeute 37.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_03
CCCN1CCc2cc(Br)ccc2C1=O
Reaction #1978434
6-bromo-2-propyl-3,4-dihydroisoquinolin-1(2H)-one
Ausbeute 71.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_08
O=C1NCCc2cc(C3CC3)ccc21
Reaction #2156971
6-Cyclopropyl-3,4-dihydro-2H-isoquinolin-1-one
Ausbeute 97.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_10
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