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16021

O=C1c2ccccc2C(=O)N1CCCl
Reaction #5368
N-(2-chloroethyl)-phthalimide
Ausbeute 65.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1CCSc1cccc2nccn12
Reaction #5546
desired product
Ausbeute 61.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2CN1CCSc1cccc2nccn12
Reaction #5569
desired product
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1CCSc1ccccn1
Reaction #6180
desired compound
Ausbeute 46.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1CCOc1ccncc1
Reaction #6244
desired compound
Ausbeute 3.1%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)CCNc1cccc(Nc2ncc(C)c(-c3sc(SC)c(C#N)c3C3CCCCC3)n2)c1
Reaction #6957
4-Cyclohexyl-5-{2-[3-(2-diethylamino-ethylamino)-phenylamino]-5-methyl-pyrimidin-4-yl}2-methylsulfanyl-thiophene-3-carbonitrile
Ausbeute 33.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C1CCN(CCN2C(=O)c3ccccc3C2=O)CC1
Reaction #10543
title compound
Ausbeute 54.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)CBr
Reaction #11575
2-bromoacetic acid N-[2-(1-adamantyl)ethyl]-N-pentylamide
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)CNCCc1ccncc1
Reaction #11576
titled compound
Ausbeute 41.6%DOI: 10.6084/m9.figshare.5104873.v1
C=CC[C@@H](NC(=O)OCc1ccccc1)C(=O)N(CC(=C)Br)Cc1ccc(OC)cc1OC
Reaction #42663
title compound
Ausbeute 58.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)CBr
Reaction #46687
2-bromoacetic acid N-[2-(1-adamantyl)ethyl]-N-pentylamide
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)CNCCc1ccncc1
Reaction #46688
compound
Ausbeute 41.6%DOI: 10.6084/m9.figshare.5104873.v1
C=CC[C@@H](NC(=O)OCc1ccccc1)C(=O)N(CC(=C)Br)Cc1ccc(OC)cc1OC
Reaction #48389
title compound
Ausbeute 58.1%DOI: 10.6084/m9.figshare.5104873.v1
C=CC[C@@H](NC(=O)OCc1ccccc1)C(=O)N(CC(=C)c1ccccc1)Cc1ccc(OC)cc1OC
Reaction #48390
title compound
Ausbeute 81.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1CC=C(Br)CNC1=O)OCc1ccccc1
Reaction #48395
title compound
Ausbeute 27.2%DOI: 10.6084/m9.figshare.5104873.v1
C=CC[C@@H](NC(=O)OCc1ccccc1)C(=O)N(CC(=C)Br)Cc1ccc(OC)cc1OC
Reaction #48406
title compound
Ausbeute 58.1%DOI: 10.6084/m9.figshare.5104873.v1
C=CC[C@@H](NC(=O)OCc1ccccc1)C(=O)N(CC(=C)c1cccc(F)c1F)Cc1ccc(OC)cc1OC
Reaction #48407
title compound
Ausbeute 69.4%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(-c2nnn(CC3CCCCN3Cc3ccccc3)n2)cc1
Reaction #58461
(RS)-1-Benzyl-2-[5-(4fluoro-phenyl)tetrazol-2-ylmethyl]-piperidine
DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(CN2CCCCC2Cn2cnc(-c3ccccc3)c2)cc1
Reaction #58462
title compound
Ausbeute 24.1%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccnc(SCCN2C(=O)c3ccccc3C2=O)n1
Reaction #63075
4-amino-2-(2-phthalimidoethylthio)pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1
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