部分構造検索

571909

O=C(CCl)N1CCCN(c2ccc([N+](=O)[O-])cc2)CC1
Reaction #8647
yellow crystals
収率 75.2%DOI: 10.6084/m9.figshare.5104873.v1
OCCN1CCN(c2ccc(N=C=S)cc2)CC1
Reaction #10877
4-(2-Hydroxyethyl)-1-(4-isothiocyanatophenyl)piperazine
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(N2CCOCC2)cc1
Reaction #46802
4-(4-Nitro-phenyl)-morpholine
DOI: 10.6084/m9.figshare.5104873.v1
O=C1COCCN1c1ccc([N+](=O)[O-])cc1
Reaction #46803
4-(4-Nitro-phenyl)-morpholin-3-one
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(N2CCOCC2=O)cc1
Reaction #46804
4-(4-Amino-phenyl)-morpholin-3-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1C(=O)C(=C(Cl)c2ccc(CN3C(=O)c4ccccc4C3=O)cc2)c2cc([N+](=O)[O-])ccc21
Reaction #53134
3-[1-chloro-1-(4-phthalimidomethyl-phenyl)-methylidene]-1-acetyl-5-nitro-2-indolinone
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1C(=O)/C(=C(\Nc2ccc(CNC(=O)OC(C)(C)C)cc2)c2ccc(CN3C(=O)c4ccccc4C3=O)cc2)c2cc([N+](=O)[O-])ccc21
Reaction #53135
(Z)-3-[1-(4-tert.butoxycarbonylaminomethyl-phenylamino)-1-(4-phthalimidomethyl-phenyl)-methylidene]-1-acetyl-5-nitro-2-indolinone
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCc1ccc(N/C(=C2\C(=O)Nc3ccc([N+](=O)[O-])cc32)c2ccc(CN)cc2)cc1
Reaction #53136
(Z)-3-[1-(4-tert.butoxycarbonylaminomethyl-phenylamino)-1-(4-aminomethyl-phenyl)-methylidene]-5-nitro-2-indolinone
DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2ccc([N+](=O)[O-])cc2/C1=C(/Nc1ccccc1)c1ccc(CN2C(=O)c3ccccc3C2=O)cc1
Reaction #53138
(Z)-3-[1-phenylamino-1-(4-phthalimidomethyl-phenyl)-methylidene]-5-nitro-2-indolinone
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCCc1ccc(N/C(=C2\C(=O)Nc3ccc([N+](=O)[O-])cc32)c2ccc(CN)cc2)cc1
Reaction #53140
(Z)-3-{1-[4-(2-tert.butoxycarbonylamino-ethyl)-phenylamino]-1-(4-aminomethyl-phenyl)-methylidene}-5-nitro-2-indolinone
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc([N+](=O)[O-])ccc1N1CCOCC1
Reaction #60926
title compound
収率 93.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)c1cc([N+](=O)[O-])ccc1N1CCOCC1
Reaction #60927
title compound
収率 93.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc([N+](=O)[O-])ccc1N1CCOCC1)N1CCN(c2ccccc2Cl)CC1
Reaction #60936
[4-(2-Chloro-phenyl)-piperazin-1-yl]-(2-morpholin-4-yl-5-nitro-phenyl)-methanone
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(N2CCN(C(=O)c3cc([N+](=O)[O-])ccc3N3CCOCC3)CC2)c(Cl)c1
Reaction #60941
3-Chloro-4-[4-(2-morpholin-4-yl-5-nitro-benzoyl)-piperazin-1-yl]-benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(N2CCN(C(=O)c3cc([N+](=O)[O-])ccc3N3CCOCC3)CC2)c(F)c1
Reaction #60973
Title compound
収率 70.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc([N+](=O)[O-])ccc1N1CCOCC1)N1CCN(c2ccc(C(F)(F)F)cc2Cl)CC1
Reaction #60982
title compound
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
N#Cc1cc(C(F)(F)F)ccc1N1CCN(C(=O)c2cc([N+](=O)[O-])ccc2N2CCOCC2)CC1
Reaction #60985
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
O=C(c1cc([N+](=O)[O-])ccc1N1CCOCC1)N1CCN(c2ccc(Cl)cc2)CC1
Reaction #60995
title compound
DOI: 10.6084/m9.figshare.5104873.v1
1 ページ次のページ