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Cn1nccc1O

Cc1cc(OC/C=C/Cl)nc(Oc2cc(C(F)(F)F)nn2C)c1
Reaction #51596
title compound
収率 52.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Cl)n(-c2ccc(Cl)nn2)n1
Reaction #56172
3-chloro-6-(3-methyl-5-chloro-1-pyrazolyl)-pyridazine
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #158162
solid
収率 51.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #158167
solid
収率 46.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N1CCN(C(=O)C(CCC(=O)OC(C)(C)C)NC(=O)c2cc(OCC(=O)N3CCCC3C(=O)OCc3ccccc3)n(-c3cccc(F)c3)n2)CC1
Reaction #176823
DOI: 10.1039/C8SC04228D
CCOC(=O)N1CCN(C(=O)C(CNC(=O)OC(C)(C)C)NC(=O)c2cc(OCC(=O)C(C)(C)C)n(-c3ccccc3)n2)CC1
Reaction #183442
DOI: 10.1039/C8SC04228D
CCOC(=O)N=Nc1cc(-c2nn(C)c(OC(F)F)c2Cl)ccc1Cl
Reaction #188250
DOI: 10.1039/C8SC04228D
CCOc1cc(OCC)c2c(c1)S(=O)(=O)N(COc1cc(C(F)(F)F)nn1-c1ccccc1)C2=O
Reaction #190291
DOI: 10.1039/C8SC04228D
CCOC(=O)N1CCN(C(=O)C(CCC(=O)OC(C)(C)C)NC(=O)c2cc(OCC(=O)N3CCCC3C(=O)O)n(-c3ccccc3)n2)CC1
Reaction #194139
DOI: 10.1039/C8SC04228D
CC(C)COc1ccc(NC(=O)c2cnn(-c3ccc(F)cc3)c2O)cc1C#N
Reaction #197537
DOI: 10.1039/C8SC04228D
CCn1nccc1Oc1cc(Sc2ccccn2)cnc1Nc1nc(C(O)C(C)(C)O)ns1
Reaction #198686
DOI: 10.1039/C8SC04228D
Cn1nc(-c2ccc(Cl)cc2Cl)cc1OC(F)F
Reaction #201518
DOI: 10.1039/C8SC04228D
O=C(NCC(=O)N1CCN(C(=O)OC2CCC2)CC1)c1cc(OCC(=O)N2CCCC2C(=O)NC2CCC2)n(-c2ccccc2)n1
Reaction #202321
DOI: 10.1039/C8SC04228D
CCOC(=O)N1CCN(C(=O)C(CC(O)CO)NC(=O)c2cc(OCC(=O)N3CCCC3C(=O)NC3CCC3)n(-c3ccccc3)n2)CC1
Reaction #211384
DOI: 10.1039/C8SC04228D
Cn1nc(-c2ccccc2)cc1C#CCCCc1ccccc1
Reaction #223806
DOI: 10.1039/C8SC04228D
COc1cc(CO)nn1-c1ccc(C(F)(F)F)cc1
Reaction #231312
DOI: 10.1039/C8SC04228D
CCOC(=O)N1CCN(C(=O)C(C)NC(=O)c2cc(OCC(=O)N3CCCC3C(=O)NC3CCC3)n(-c3ccccc3)n2)CC1
Reaction #237570
DOI: 10.1039/C8SC04228D
Cn1nc(-c2ccccc2)cc1C#CC1=CCCCC1
Reaction #239955
DOI: 10.1039/C8SC04228D
CCn1ncc(C(=O)c2cc(C)c3c(c2Cl)C(=O)C(C)(C)CS3(=O)=O)c1OS(=O)(=O)c1ccc(C)cc1
Reaction #241602
DOI: 10.1039/C8SC04228D
CCn1nccc1Oc1cc(Sc2ccccn2)cnc1C#N
Reaction #252971
DOI: 10.1039/C8SC04228D
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