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786386

CN1CCc2cccc(Nc3cc(Cl)ncc3Cl)c2C1=O
Reaction #118
Ausbeute 42.5%
CN1CCc2cccc(Nc3cc(Cl)ncc3Cl)c2C1=O
Reaction #119
Ausbeute 63.3%
CN1CCc2cccc(Nc3cc(Cl)ncc3Cl)c2C1=O
Reaction #120
Ausbeute 49.4%
CN1CCc2cccc(Nc3cc(Cl)ncc3Cl)c2C1=O
Reaction #121
Ausbeute 59.5%
Cc1nn(C)cc1Nc1cc(Nc2cccc3c2C(=O)N(C)CC3)c(C#N)cn1
Reaction #131
Ausbeute 7.3%
Cc1nn(C)cc1Nc1cc(Nc2cccc3c2C(=O)N(C)CC3)c(C#N)cn1
Reaction #132
Ausbeute 54.9%
Cc1nn(C)cc1Nc1cc(Nc2cccc3c2C(=O)N(C)CC3)c(C#N)cn1
Reaction #133
Ausbeute 43.8%
Cc1nn(C)cc1Nc1cc(Nc2cccc3c2C(=O)N(C)CC3)c(C#N)cn1
Reaction #134
Ausbeute 15.6%
Cc1nn(C)cc1Nc1cc(Nc2cccc3c2C(=O)N(C)CC3)c(C#N)cn1
Reaction #178
Ausbeute 33.2%
CN1CCc2cccc(Nc3cc(Nc4ccnn4C)ncc3Cl)c2C1=O
Reaction #219
Ausbeute 48.0%
CN1CCc2cccc(Nc3cc(Nc4ccnn4C)ncc3Cl)c2C1=O
Reaction #220
Ausbeute 43.8%
CN1CCc2cccc(Nc3cc(Nc4ccnn4C)ncc3Cl)c2C1=O
Reaction #221
Ausbeute 26.9%
CN1CCc2cccc(Nc3cc(Nc4ccnn4C)ncc3Cl)c2C1=O
Reaction #222
Ausbeute 30.3%
CN1CCc2cccc(Nc3cc(Nc4ccnn4C)ncc3Cl)c2C1=O
Reaction #223
Ausbeute 69.8%
Cc1nn(C)cc1Nc1cc(Nc2cccc3c2C(=O)N(C)CC3)c(C(F)(F)F)cn1
Reaction #234
Ausbeute 33.7%
COc1ccc(N2CCN(C)CC2)c2c1CCN(C(=O)Cc1ccc(N3CCCCC3)cc1)C2
Reaction #708
Ausbeute 0.0%
CCN1CCc2c(Br)ccc(NC(C)=O)c2C1
Reaction #76489
acetamide
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1ccc(Br)c2c1CN(C)CC2
Reaction #76499
desired product
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCc2c(Br)cc(N)c(N)c2C1
Reaction #76500
5-Bromo-1,2,3,4-tetrahydro-2-methyl-7,8-isoquinolinediamine
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCc2c(c([N+](=O)[O-])cc3[nH]c(=O)c(=O)[nH]c23)C1.CS(=O)(=O)O
Reaction #76520
title compound
Ausbeute 35.0%DOI: 10.6084/m9.figshare.5104873.v1
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