3-(4-fluorobenzoyl)-8-hydroxy-1,1-dimethyl-1,2,3,6-tetrahydroazepino[4,5-b]indole-5-carboxylic acid ethyl ester

CCOC(=O)C1=CN(C(=O)c2ccc(F)cc2)CC(C)(C)c2c1[nH]c1cc(OC(=O)N(C)C)ccc21
Reaction #66233
title compound
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(=O)C1=CN(C(=O)c2ccc(F)cc2)CC(C)(C)c2c1[nH]c1cc(OC(=O)NCCN(C)C)ccc21
Reaction #66235
title compound
Ausbeute 28.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(=O)C1=CN(C(=O)c2ccc(F)cc2)CC(C)(C)c2c1[nH]c1cc(OCCN3CCOCC3)ccc21
Reaction #66236
title compound
Ausbeute 10.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(=O)C1=CN(C(=O)c2ccc(F)cc2)CC(C)(C)c2c1[nH]c1cc(OCCN3CCOCC3)ccc21
Reaction #66237
3-(4-Fluorobenzoyl)-1,1-Dimethyl-8-(2-Morpholin-4-yl-Ethoxy)-1,2,3,6-Tetrahydroazepino[4,5-b]Indole-5-Carboxylic Acid Ethyl Ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(=O)C1=CN(C(=O)c2ccc(F)cc2)CC(C)(C)c2c1[nH]c1cc(OC(=O)N(C)C)ccc21
Reaction #823271
title compound
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_09
CCOC(=O)C1=CN(C(=O)c2ccc(F)cc2)CC(C)(C)c2c1[nH]c1cc(OC(=O)NCCN(C)C)ccc21
Reaction #823273
title compound
Ausbeute 28.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_09
CCOC(=O)C1=CN(C(=O)c2ccc(F)cc2)CC(C)(C)c2c1[nH]c1cc(OCCN3CCOCC3)ccc21
Reaction #823274
title compound
Ausbeute 10.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_09
CCOC(=O)C1=CN(C(=O)c2ccc(F)cc2)CC(C)(C)c2c1[nH]c1cc(OCC(N)=O)ccc21
Reaction #823275
8-carbamoylmethoxy-3-(4-fluorobenzoyl)-1,1-dimethyl-1,2,3,6-tetrahydroazepino[4,5-b]indole-5-carboxylic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_09
CCOC(=O)C1=CN(C(=O)c2ccc(F)cc2)CC(C)(C)c2c1[nH]c1cc(OC(=O)N(C)C)ccc21
Reaction #918074
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CCOC(=O)C1=CN(C(=O)c2ccc(F)cc2)CC(C)(C)c2c1[nH]c1cc(OCCN3CCOCC3)ccc21
Reaction #1023429
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
CCOC(=O)C1=CN(C(=O)c2ccc(F)cc2)CC(C)(C)c2c1[nH]c1cc(OC(=O)N(C)C)ccc21
Reaction #1181774
title compound
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_03
CCOC(=O)C1=CN(C(=O)c2ccc(F)cc2)CC(C)(C)c2c1[nH]c1cc(OC(=O)NCCN(C)C)ccc21
Reaction #1181776
title compound
Ausbeute 28.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_03
CCOC(=O)C1=CN(C(=O)c2ccc(F)cc2)CC(C)(C)c2c1[nH]c1cc(OCCN3CCOCC3)ccc21
Reaction #1181777
title compound
Ausbeute 10.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_03
CCOC(=O)C1=CN(C(=O)c2ccc(F)cc2)CC(C)(C)c2c1[nH]c1cc(OCC(N)=O)ccc21
Reaction #1181778
8-carbamoylmethoxy-3-(4-fluorobenzoyl)-1,1-dimethyl-1,2,3,6-tetrahydroazepino[4,5-b]indole-5-carboxylic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_03
CCOC(=O)C1=CN(C(=O)c2ccc(F)cc2)CC(C)(C)c2c1[nH]c1cc(OC(=O)N(C)C)ccc21
Reaction #1810949
title compound
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_02
CCOC(=O)C1=CN(C(=O)c2ccc(F)cc2)CC(C)(C)c2c1[nH]c1cc(OC(=O)NCCN(C)C)ccc21
Reaction #1810951
title compound
Ausbeute 28.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_02
CCOC(=O)C1=CN(C(=O)c2ccc(F)cc2)CC(C)(C)c2c1[nH]c1cc(OCCN3CCOCC3)ccc21
Reaction #1810952
title compound
Ausbeute 10.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_02
CCOC(=O)C1=CN(C(=O)c2ccc(F)cc2)CC(C)(C)c2c1[nH]c1cc(OCCN3CCOCC3)ccc21
Reaction #1810953
3-(4-fluorobenzoyl)-1,1-dimethyl-8-(2-morpholin-4-yl-ethoxy)-1,2,3,6-tetrahydroazepino[4,5-b]indole-5-carboxylic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_02