Participa en 201 reacciones

9073

COc1ccc(CS[C@H]2C[C@@H](C(N)=O)N(CCO)C2)cc1
Reaction #5206
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CNC(=O)[C@@H]1C[C@H](SCc2ccc(OC)cc2)CN1CCO
Reaction #5210
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
OCCn1cc(-c2cnc3nnn(Cc4cc5cccnc5cc4F)c3n2)cn1
Reaction #44293
desired product
Rendimiento 31.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cc(OC)c(Cl)c(-c2ccc(C(=O)Nc3ccc(CN4CCN(CCO)CC4)cn3)c3nccnc23)c1Cl
Reaction #71412
title compound
Rendimiento 76.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
OCCN1CCN(c2ccccc2F)CC1
Reaction #77309
title compound
Rendimiento 65.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
Cc1noc(C(C)NC(=O)c2cc3c(-c4ccc(F)cc4F)nn(CCO)c3s2)n1
Reaction #190210
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(Nc1ccc(Cl)cc1)c1cccn(C2CCc3c2cccc3N2CCN(CCO)CC2)c1=O
Reaction #200530
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(Nc1ccc(Cl)cc1)c1oc2ccccc2c1NC(=O)C1CCC(NCCO)CC1
Reaction #201714
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COCCC1CN(C2=Nc3ccccc3Nc3sc(C(F)(F)F)nc32)CCN1CCO
Reaction #218689
title compound
Rendimiento 26.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CN(CCO)C1CCC(C(=O)Nc2c(C(=O)Nc3ccc(Cl)cn3)oc3ccccc23)CC1
Reaction #223698
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(=O)c1cccc(C2CCN(CCO)CC2)c1F
Reaction #267151
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1ccc(F)cc1C1NC(=O)CC(c2cc(Cl)ccc2N2CCN(CCO)CC2)C12C(=O)Nc1cc(Cl)ccc12
Reaction #269676
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC1(C)CC(OC(=O)c2ccccc2)CC(C)(C)N1OCCO
Reaction #270294
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=c1oc2cc(N3CCN(CCO)CC3)ccc2cc1-c1nc2ccccc2s1
Reaction #287411
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1nc(C#Cc2ccnc(Cl)c2)c(C)n1-c1ccn(CCO)c(=O)c1
Reaction #289310
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOC(=O)c1oc2cccc(OCCO)c2c1C
Reaction #297568
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CNC(=O)C1CC(SCc2ccc(OC)cc2)CN1CCO
Reaction #301925
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCC(CCC)C(=O)O
Reaction #347384
valproic acid
Rendimiento 138.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_06
O=C1CCC(c2cccc(OCCO)c2)N1c1cnc(Oc2ccc(Cl)cc2)cn1
Reaction #374489
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COc1cc(C=O)cc(OC)c1OCCO
Reaction #422534
4-hydroxyethyloxy-3,5-dimethoxybenzaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
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