Substructure Search

763163

CC(=O)OCc1nc(C(Cl)Cl)cnc1N1C(=O)c2ccccc2C1=O
Reaction #4535
3-acetoxymethyl-5-dichloromethyl-2-phthalimidopyrazine
Yield 77.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1c1ncc(C(Cl)Cl)nc1CO
Reaction #4536
5-dichloromethyl-3-hydroxymethyl-2-phthalimidopyrazine
Yield 54.0%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1nc(C(Cl)Cl)cnc1N1C(=O)c2ccccc2C1=O
Reaction #4537
colorless crystals
Yield 78.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1C1N=CC(C(Cl)Cl)=NC1=NO
Reaction #4538
colorless crystals
Yield 67.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1c1ncc(C(Cl)Cl)nc1CO
Reaction #4540
5-dichloromethyl-3-hydroxymethyl-2-phthalimidopyrazine
Yield 47.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCCSc1ccncc1)c1cnc2ccccc2n1
Reaction #6269
desired compound
Yield 48.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ncc(CCl)nc1C
Reaction #48020
(Chloromethyl)dimethylpyrazine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cnc(CN2CCNC2=C[N+](=O)[O-])cn1
Reaction #50492
1-(2-methyl-5-pyrazinylmethyl)-2-(nitromethylene)imidazolidine
Yield 23.0%DOI: 10.6084/m9.figshare.5104873.v1
NCCNCc1cnccn1
Reaction #50504
N-(pyrazinylmethyl)ethylenediamine
Yield 92.3%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(=NC(Cl)c2cnccn2)n(-c2c(Cl)cc(C(F)(F)F)cc2Cl)[nH]1
Reaction #51142
1-(2,6-dichloro-4-trifluoromethylphenyl)-5-(pyrazin-2-ylchloromethylimino)pyrazole-3-carbonitrile
Yield 79.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(NCc2cnccn2)n(-c2c(Cl)cc(C(F)(F)F)cc2Cl)n1
Reaction #51143
1-(2,6-dichloro-4-trifluoromethylphenyl)-5-(pyrazin-2-ylmethylamino)pyrazole-3-carbonitrile
Yield 92.4%DOI: 10.6084/m9.figshare.5104873.v1
Cl.NCCSCc1cnccn1
Reaction #55121
2-[(2-aminoethyl)thiomethyl]pyrazine hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cl.NCCSCc1cnccn1
Reaction #55786
2-[(2-aminoethyl)thiomethyl]pyrazine hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
OCCOCc1cnccn1
Reaction #55792
2-(2-hydroxyethoxymethyl)pyrazine
DOI: 10.6084/m9.figshare.5104873.v1
NCCNCc1cnccn1
Reaction #55801
N-(2-pyrazinylmethyl)ethylenediamine
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=NCCNCc1cnccn1)NC#N
Reaction #55803
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Fc1cc(OCc2cnc3ccccc3n2)ccc1-c1nn(CC(F)(F)F)cc1-c1ccncc1
Reaction #62183
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(-c2cnco2)cc1)N(C1CC1)C1CCN(c2noc(-c3cnccn3)n2)CC1
Reaction #156028
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(c1nc2ccc(F)cc2nc1Cl)N1C(=O)c2ccccc2C1=O
Reaction #162568
2-(1-(3-chloro-6-fluoroquinoxalin-2-yl)ethyl)isoindoline-1,3-dione
Yield 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1nc2c(cnn2CC)nc1C(=O)Nc1nccs1
Reaction #173953
DOI: 10.1039/C8SC04228D
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