Участвует в 1259 реакциях

5558

CCNC(=O)Nc1nc2nc(N)ncc2cc1-c1c(Cl)cccc1Cl
Reaction #3514
1-[2-amino-6-(2,6-dichlorophenyl)-pyrido[2,3-d]pyrimidin-7-yl]-3-ethylurea
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCNC(=O)Nc1nc2nc(NCCCN3CCN(C)CC3)ncc2cc1-c1c(Cl)cccc1Cl
Reaction #3531
1-{6-(2,6-dichlorophenyl)-2-[3-(4-methyl-piperazin-1-yl)-propylamino]-pyrido-[2,3-d]pyrimidin-7-yl}-3-ethyl-urea
Выход 74.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCNC(=O)Nc1nc2nc(NCCCCN(CC)CC)ncc2cc1-c1c(Cl)cccc1Cl
Reaction #3579
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCNC(=O)NNC(=S)NCCCOc1cccc(CN2CCCCC2)c1
Reaction #4706
N-Ethyl-2-[[3-[3-(1-piperidinylmethyl)phenoxy]propyl]aminothioxomethyl]-hydrazine carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CCNC(=O)Nc1nc2ccc(Cl)cc2s1
Reaction #9194
N-(6-Chloro-1,3-benzothiazol-2-yl)-N′-ethylurea
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCNC(=O)Nc1nc2ccc(C#N)cc2s1
Reaction #9199
N-(6-Cyano-1,3-benzothiazol-2-yl)-N′-ethylurea
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCNC(=O)Nc1nc2c(s1)C(=O)CCC2
Reaction #9202
4
Выход 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCNC(=O)Nc1nc2ccc(Cc3ccccc3)cc2s1
Reaction #9222
desired compound
Выход 56.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCNC(=O)Nc1nc2ccc(Br)cc2s1
Reaction #9224
desired compound
Выход 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCNC(=O)Nc1nc2ccc(C(=O)OCC)cc2s1
Reaction #9232
desired compound
Выход 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCNC(=O)Nc1nc2ccc(C#N)cc2s1
Reaction #9264
N-(6-Cyano-1,3-benzothiazol-2-yl)-N′-ethylurea
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCNC(=O)Nc1nc2ccc(Br)cc2s1
Reaction #9267
N-(6-Bromo-1,3-benzothiazol-2-yl)-N′-ethylurea
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCNC(=O)Nc1nc2c(C#N)cc(C)cc2s1
Reaction #9273
N-(6-Methylcyano-1,3-benzothiazol-2-yl)-N′-ethylurea
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCNC(=O)NCc1cccc2c1C(=O)N(C1CCC(=O)NC1=O)C2=O
Reaction #10072
N-{[2-(2,6-dioxo(3-piperidyl))-1,3-dioxoisoindolin-4-yl]methyl}(ethylamino)carboxamide
Выход 30.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCNC(=O)NCc1cccc2c1CN(C1CCC(=O)NC1=O)C2=O
Reaction #10162
N-{[2-(2,6-dioxo(3-piperidyl))-1-oxoisoindolin-4-yl]methyl}(ethylamino)carboxamide
Выход 42.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCNC(=O)OCc1ccc2c(n1)N1[C@H](C2)CN(C(=O)OC(C)(C)C)C[C@H]1C
Reaction #12057
title compound
Выход 215.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCNC(=O)O[C@]1(C(=O)COC(C)=O)[C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O[Si](C)(C)C)C[C@@]21C
Reaction #42652
title compound
Выход 62.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCNC(=O)N[C@H]1CC[C@H](CCN2CCN(c3cccc(Cl)c3Cl)CC2)CC1
Reaction #44399
title compound
Выход 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCNC(=O)Nc1cccc(-c2ccc3c(c2)CC(NS(=O)(=O)C(C)C)C3)c1
Reaction #46702
title compound
Выход 24.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCNC(=O)NCCCOc1cc(I)c2c(c1Cl)CNC2=O
Reaction #49607
4-chloro-5-[3-(ethylcarbamoylamino)propoxy]-7-iodoisoindolinone
Выход 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
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