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Nc1ccc(N2CCOCC2)cc1

Cc1cc(N2CCOCC2)cc(C)c1NC(=O)CC(C)(C)C
Reaction #303
Выход 63.7%
COc1cccc(-c2ccc3c(c2)NC(=O)C3=CNc2ccc(N3CCOCC3)cc2)c1
Reaction #11634
compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1cccc(-c2cncc(Nc3ccc(N4CCOCC4)cc3)n2)c1
Reaction #44545
pure title compound
Выход 29.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc2c1nc(C(=O)Nc1ccc(N3CCOCC3=O)cc1)n2CC(=O)Nc1ccc(Cl)cn1
Reaction #46807
1-[(5-Chloro-pyridin-2-ylcarbamoyl)-methyl]-2-[4-(3-oxo-morpholin-4-yl)-phenylcarbamoyl]-1H-benzoimidazole-4-carboxylic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cn1c(C(=O)Nc2ccc(N3CCOCC3=O)cc2)nc2c(C(=O)O)cccc21)Nc1ccc(Cl)cn1
Reaction #46821
1-[(5-Chloro-pyridin-2-ylcarbamoyl)-methyl]-2-[4-(3-oxo-morpholin-4-yl)-phenylcarbamoyl]-1H-benzoimidazole-4-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
O[C@@H](CCl)CNc1ccc(N2CCOCC2)c(F)c1
Reaction #46943
N-[3-Chloro-2-(R)-hydroxypropyl]-3-fluoro-4-morpholinyl aniline
Выход 99.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2ccc([N+](=O)[O-])cc2/C1=C(/Nc1ccc(N2CCOCC2)cc1)c1ccccc1
Reaction #53078
(Z)-3-[1-(4-morpholinophenylamino)-1-phenyl-methylidene]-5-nitro-2-indolinone
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(c2ccc(N3CCN(C(=O)OC(C)(C)C)CC3)c(C3CCC(C)(C)CC3)c2)C[C@H](C)O1
Reaction #60456
title compound
Выход 86.1%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(c2ccc(N3CCNCC3)c(C3CCC(C)(C)CC3)c2)C[C@H](C)O1
Reaction #60457
title compound
Выход 87.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(N2CCN(C(=O)c3cc([N+](=O)[O-])ccc3N3CCOCC3)CC2)c(F)c1
Reaction #60973
Title compound
Выход 70.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc([N+](=O)[O-])ccc1N1CCOCC1)N1CCN(c2ccc(OC(F)(F)F)cc2)CC1
Reaction #60984
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(N2CCN(C(=O)c3cc([N+](=O)[O-])ccc3N3CCOCC3)CC2)cc1
Reaction #60987
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1ccc(N2CCN(C(=O)c3cc([N+](=O)[O-])ccc3N3CCOCC3)CC2)cc1
Reaction #60990
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc([N+](=O)[O-])ccc1N1CCOCC1)N1CCN(c2ccc(F)cc2F)CC1
Reaction #61007
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc([N+](=O)[O-])ccc1N1CCOCC1)N1CCN(c2nsc3ccccc23)CC1
Reaction #61463
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #62018
Formula IV
DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1C[C@H](O)CNc1ccc(N2CCOCC2)c(F)c1
Reaction #62019
N-[3-pthalimido-2-(R)-hydroxypropyl]-3-fluoro-4-(morpholinyl)aniline
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(N2CCOCC2)cc(N)c1N
Reaction #72799
desired product
Выход 80.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(N2CCOCC2)cc2nc(C(F)(F)F)[nH]c12
Reaction #72800
desired product
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(N2CCOCC2)cc2[nH]c(=O)[nH]c12
Reaction #72821
desired product
Выход 62.0%DOI: 10.6084/m9.figshare.5104873.v1
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