4-morpholinoacetophenone

O=C(CBr)c1ccc(N2CCOCC2)cc1
Reaction #10881
2-Bromo-1-[4-(4-morpholinyl)phenyl]ethanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
c1cc(-c2ccc(N3CCOCC3)cc2)n[nH]1
Reaction #40710
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(CC(=O)C(F)F)c1ccc(N2CCOCC2)cc1
Reaction #216389
solid
Yield 91.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
O=C(CBr)c1ccc(N2CCOCC2)cc1
Reaction #241024
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(C)OC(=O)Nc1ccccc1NC(=O)c1ccc(C=CC(=O)c2ccc(N3CCOCC3)cc2)cc1
Reaction #278361
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(CBr)c1ccc(N2CCOCC2)cc1
Reaction #440906
2-Bromo-1-[4-(4-morpholinyl)phenyl]ethanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_06
O=C(CC(=O)C(F)F)c1ccc(N2CCOCC2)cc1
Reaction #527244
solid
Yield 91.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_05
O=C(CC(=O)C(F)F)c1ccc(N2CCOCC2)cc1
Reaction #528224
solid
Yield 91.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_05
O=C(CC(=O)C(F)F)c1ccc(N2CCOCC2)cc1
Reaction #951721
solid
Yield 91.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_10
CC(=O)c1ccc(N2CCOCC2)cc1
Reaction #1101965
52b
Yield 74.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_07
CC(C)(C)OC(=O)Nc1ccccc1NC(=O)c1ccc(C=CC(=O)c2ccc(N3CCOCC3)cc2)cc1
Reaction #1267994
title compound
Yield 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_10
O=C(CC(=O)C(F)F)c1ccc(N2CCOCC2)cc1
Reaction #1378746
solid
Yield 91.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_05
COC(=O)C=C(C)c1ccc(N2CCOCC2)cc1
Reaction #1587437
3-(4-morpholinophenyl)but-2-enoic acid methyl ester
Yield 69.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_12
COC(=O)C=C(C)c1ccc(N2CCOCC2)cc1
Reaction #1590375
3-(4-morpholinophenyl)but-2-enoic acid methyl ester
Yield 69.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_12
O=C(CC(=O)C(F)F)c1ccc(N2CCOCC2)cc1
Reaction #1625927
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
c1cc(-c2ccc(N3CCOCC3)cc2)n[nH]1
Reaction #1802350
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_09
O=C(CC(=O)C(F)F)c1ccc(N2CCOCC2)cc1
Reaction #1808293
solid
Yield 91.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_04
O=C(O)c1ccc2c(c1)nc(-c1ccc3nc(-c4ccc(N5CCOCC5)cc4)ccc3c1)n2C1CCCCC1
Reaction #1875676
title compound
Yield 30.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_03
c1cc(-c2ccc(N3CCOCC3)cc2)n[nH]1
Reaction #2176465
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_05
CC(=O)c1ccc(N2CCOCC2)cc1
Reaction #2207450
title-compound
Yield 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_02
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