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343246

Cl.N#Cc1cncc2cccc(O[C@H]3CC[C@H](N)CC3)c12
Reaction #10663
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.N#Cc1cncc2cccc(O[C@H]3CC[C@H](NCCO)CC3)c12
Reaction #10685
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@H]1CN2CCC1CC2)c1nsc2cc(N3CCOCC3)ccc12
Reaction #62029
6-morpholin-4-ylbenzo[d]isothiazole-3-carboxylic acid ((3R)-1-azabicyclo[2.2.2]oct-3-yl)amide
Ausbeute 180.3%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)C(=O)N[C@H]1C[C@@H]2c3cc(CO)cc4[nH]c(C)c(c34)C[C@H]2N(C)C1
Reaction #64130
1,1-Diethyl-3-(2,6-dimethyl-13-hydroxymethyl-8alpha-ergolinyl)-urea
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)C(=O)N[C@H]1C[C@@H]2c3cc(C)cc4[nH]c(C)c(c34)C[C@H]2N(C)C1
Reaction #64131
1,1-Diethyl-3-(2,6,13-trimethyl-8alpha-ergolinyl)-urea
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)C(=O)N[C@H]1C[C@@H]2c3cc(C)cc4[nH]c(C)c(c34)C[C@H]2N(C)C1
Reaction #64132
1,1-Diethyl-3-(2,6,13-trimethyl-8alpha-ergolinyl)-urea
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)C(=S)N[C@H]1C[C@@H]2c3cc(C)cc4[nH]c(C)c(c34)C[C@H]2N(C)C1
Reaction #64138
1,1-Diethyl,3-(2,6,13-trimethyl-8alpha-ergolinyl)-thiourea
Ausbeute 43.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1CCCCC1)c1c(O)c2ccccc2[nH]c1=O
Reaction #72682
N-cyclohexyl-4-hydroxy-2-oxo-1,2-dihydroquinoline-3-carboxamide
Ausbeute 35.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(=Cc1ccc(C#N)cc1OC[C@H](N)CCC(=O)OCc1ccccc1)NC(C)=O.Cl
Reaction #78203
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(N2C[C@H]3C[C@H]3C2C(N)=O)ncc1-c1cc(C(F)(F)F)cc2[nH]ncc12
Reaction #86400
title compound
Ausbeute 3.2%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)CN1CCOCC1)C(=O)N[C@@H](CCc1ccccc1)C(=O)OCc1ccccc1
Reaction #87072
(S)-benzyl 2-((S)-2-(2-morpholinoacetamido)propanamido)-4-phenylbutanoate
Ausbeute 71.3%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CCCN[C@H]1CNC(=O)c1cccc2cccnc12
Reaction #89070
rac-cis-N-((3-Methylpiperidin-2-yl)methyl)quinoline-8-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
OC1C2CCN(CC2)C1C(c1ccccc1)c1cccnc1
Reaction #192051
DOI: 10.1039/C8SC04228D
CC(NC(=O)C(N)CCCC(NC(=O)OCc1ccccc1)C(=O)OCc1ccccc1)C(=O)OCc1ccccc1
Reaction #196839
DOI: 10.1039/C8SC04228D
O=C(CCC(=O)C(Cc1ccccc1)NC(=O)c1ccccc1)NC(Cc1ccccc1)C(=O)O
Reaction #198194
DOI: 10.1039/C8SC04228D
CCN(CC)C(=O)NC1CC2c3cccc4c3c(c(C)n4C)CC2N(C)C1
Reaction #210837
DOI: 10.1039/C8SC04228D
CCN(CC)C(=O)NC1CC2c3cccc4[nH]c(CO)c(c34)CC2N(C)C1
Reaction #213070
DOI: 10.1039/C8SC04228D
O=C(NC1CCC(C(F)(F)F)CC1)c1cc([N+](=O)[O-])c(Cl)nc1OCCF
Reaction #213295
DOI: 10.1039/C8SC04228D
N#Cc1ccc2[nH]c3c(c2c1)CC(N1C(=O)c2ccccc2C1=O)CC3
Reaction #215931
3-phthalimido-6-cyano-1,2,3,4-tetrahydrocarbazole
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2[nH]c3c(c2c1)CC(N1C(=O)c2ccccc2C1=O)CC3
Reaction #215932
3-phthalimido-6-methoxy-1,2,3,4-tetrahydrocarbazole
Ausbeute 93.5%DOI: 10.6084/m9.figshare.5104873.v1
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