部分構造検索

1173531

Nc1cc(Cl)c([N+](=O)[O-])cc1Cl
Reaction #4327
2,5-dichloro-4-nitroaniline
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(NCCO)c(Cl)cc1[N+](=O)[O-]
Reaction #4333
2-amino-4-β-hydroxyethylamino-5-chloronitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1
NCCNc1cc(NCCO)c(Cl)cc1[N+](=O)[O-]
Reaction #4335
2-chloro-5-β-aminoethylamino-4-nitro-N-(β-hydroxyethyl)aniline
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(NCC2CCCO2)c(Cl)c1
Reaction #54619
2-chloro-4-nitro-N-tetrahydrofurfurylaniline
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Nc1ccc(NCC2CCCO2)c(Cl)c1
Reaction #54620
2-chloro-4-amino-N-tetrahydrofurfurylaniline monohydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc([N+](=O)[O-])c(N)c(Cl)c1Nc1ccccc1
Reaction #60310
pure desired product
収率 84.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(N)c(N)c(Cl)c1Nc1ccccc1
Reaction #60311
clean desired product
収率 70.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2ccc([N+](=O)[O-])cc2Cl)CC1
Reaction #60501
title compound
収率 64.7%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C=C(c2cc([N+](=O)[O-])ccc2N2CCN(C(=O)OC(C)(C)C)CC2)CC(C)(C)C1
Reaction #60502
title compound
収率 14.1%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)c1ccc([N+](=O)[O-])cc1Cl
Reaction #60638
3-chloro-4-(dimethylamino) nitrobenzene
収率 101.1%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cc(Cl)c(I)c(Cl)c1
Reaction #63565
3,5-dichloro-4-iodonitrobenzene
収率 86.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2ccc(N)cc2Cl)CC1
Reaction #66528
tert-butyl 4-(4-amino-2-chlorophenyl)piperazine-1-carboxylate
収率 98.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC(=O)Nc1ccc([N+](=O)[O-])cc1Cl
Reaction #74772
2'-Chloro-4'-nitrovaleranilide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(=O)NNc1ccc([N+](=O)[O-])cc1Cl
Reaction #75001
desired product
収率 90.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(OC[C@@H]2C[C@@H](O)CN2C(=O)OCCNCCc2ccc(N=Nc3ccc([N+](=O)[O-])cc3Cl)cc2)(c2ccccc2)c2ccc(OC)cc2)cc1
Reaction #76238
2-({4-[(2-Chloro-4-nitrophenyl)diazenyl]phenyl}ethylamino)ethyl (5S,3R)-5-{[bis(4-methoxyphenyl)phenylmethoxy]methyl}-3-hydroxypyrrolidinecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(OC[C@@H]2C[C@@H](OP(OCCC#N)N(C(C)C)C(C)C)CN2C(=O)OCCNCCc2ccc(N=Nc3ccc([N+](=O)[O-])cc3Cl)cc2)(c2ccccc2)c2ccc(OC)cc2)cc1
Reaction #76239
2-({4-[(2-Chloro-4-nitrophenyl)diazenyl]phenyl}ethylamino)ethyl (2S,4R)-2-{[bis(4-methoxyphenyl)phenylmethoxy]methy}-4-{[bis(methylethyl)amino](2-cyano-ethoxy)phosphinooxy}pyrrolidinecarboxylate
収率 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCCN(CCCO)c1ccc(N=Nc2ccc([N+](=O)[O-])cc2Cl)cc1
Reaction #76242
Ethyl 4-({4-[(2-chloro-4-nitrophenyl)diazenyl]phenyl}(3-hydroxypropyl)amino)-butanoate
収率 68.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCCN(CCCO)c1ccc(N=Nc2ccc([N+](=O)[O-])cc2Cl)cc1
Reaction #76243
4-({4-[(2-Chloro-4-nitrophenyl)diazenyl]phenyl}(3-hydroxypropyl)amino)butanoic Acid
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(Cc1ccc2ccccc2c1)Nc1ccc([N+](=O)[O-])cc1Cl
Reaction #84500
title compound
収率 43.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(Cc1ccc2ccccc2c1)Nc1ccc(N)cc1Cl
Reaction #84501
title compound
収率 84.7%DOI: 10.6084/m9.figshare.5104873.v1
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