子结构搜索

Cl.N=C(N)Cl

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Reaction #1801
solid
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(NC23N=CN=C2C=NC(Cl)=N3)n[nH]1
Reaction #11928
(2-chloro-purin-4-yl)-(5-methyl-1H-pyrazol-3-yl)-amine
收率 58.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=Nc1ccccc1)N(C)OCCCN1CCCCC1
Reaction #48031
title compound
收率 10.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC12CCC(c3nnc(-c4ccc(OC)cc4C)o3)(CC1)CC2
Reaction #51109
2-(4-methoxy-2-methylphenyl)-5-(4-pentylbicyclo[2.2.2]oct-1-yl)-1,3,4-oxadiazole
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1Cc2nc(Cl)nc(Nc3ccc(F)c(Cl)c3)c2N=C1Cl
Reaction #51438
1-[2,6-Dichloro-8-(3-chloro-4-fluorophenylamino)-4H-pyrimido[5,4-d]pyrimidin-3-yl]ethanone
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1Cc2nc(Cl)nc(Nc3ccc(F)c(Cl)c3)c2N=C1NC1CCN(C)CC1
Reaction #51439
1-[6-chloro-8-(3-chloro-4-fluorophenylamino)-2-(1-methylpiperidin-4-ylamino)-4H-pyrimido[5,4-d]pyrimidin-3yl]ethanone
DOI: 10.6084/m9.figshare.5104873.v1
OC[C@H]1O[C@@H](n2cnc3c(NC4CCCC4)nc(Cl)nc32)[C@H](O)[C@@H]1O
Reaction #58778
2-chloro-N6-cyclopentyladenosine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(NC23N=CN=C2C=NC(Cl)=N3)n[nH]1
Reaction #66470
(2-chloro-purin-4-yl)-(5-methyl-1H-pyrazol-3-yl)-amine
收率 58.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(=Cc1ccc(C#N)cc1OC[C@@H](CCC(=O)OCc1ccccc1)NC(=O)c1cccc(-c2ccc(NC(=N)N)cc2)c1)NC(C)=O.O=C(O)C(F)(F)F
Reaction #78214
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(N)c2c(Cl)c(-c3cc(Cl)cc(Cl)c3)ccc2n1
Reaction #80905
2,4-diamino-5-chloro-6-(3,5-dichlorophenyl)quinazoline
收率 29.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C(Cl)=Cc2ccc(C(F)(F)F)cc2)ccc2nc(N)nc(N)c12
Reaction #80919
2,4-diamino-5-methyl-6-[1-chloro-2-(4-trifluoromethylphenyl)ethenyl]quinazoline
收率 46.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc2nc(N)nc(N)c12
Reaction #80935
2,4-diamino-5-methylquinazoline
收率 86.9%DOI: 10.6084/m9.figshare.5104873.v1
CN=C=Nc1ccccc1
Reaction #96062
carbodiimide
DOI: 10.6084/m9.figshare.5104873.v1
CNC(Cl)=Nc1ccccc1.Cl
Reaction #96063
N-Methyl-N'-phenyl-chloroformamidine hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
ClCCN1C(Cl)=Nc2ccc(Cl)cc2C1c1ccccc1
Reaction #204350
DOI: 10.1039/C8SC04228D
Cc1cc(NC23N=CN=C2C=NC(Cl)=N3)n[nH]1
Reaction #220339
(2-chloro-purin-4-yl)-(5-methyl-1H-pyrazol-3-yl)-amine
收率 58.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C2=Nc3ccc(Cl)cc3S(=O)(=O)N2)CC1
Reaction #239082
DOI: 10.1039/C8SC04228D
O=S1(=O)N=C(NCCC(c2ccccc2)c2ccccc2)Nc2ccc(Cl)cc21
Reaction #256860
DOI: 10.1039/C8SC04228D
CN(C)C(Cl)=Nc1ccc(Cl)c(Cl)c1
Reaction #258414
DOI: 10.1039/C8SC04228D
CCCN1CCN2C1=Nc1ccc(Cl)cc1C2c1ccccc1
Reaction #273354
DOI: 10.1039/C8SC04228D
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