部分構造検索

Nc1nccnc1Cl

Cc1ccccc1COc1nccnc1N
Reaction #4389
2-amino-3-(2-methylbenzyloxy)pyrazine
収率 41.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1CNc1nccnc1N
Reaction #4390
2-amino-3-(2-methylbenzylamino)pyrazine
収率 19.7%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(Nc1nc2ccccc2nc1Cl)c1ccccc1Cl
Reaction #42693
title compound
収率 101.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(F)cc1)c1n[nH]cc1Nc1nccnc1Cl
Reaction #48568
title compound
収率 19.6%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N=C(NCCCCc1ccc(O)cc1)NC(=O)c1nc(Cl)c(N)nc1N
Reaction #53369
4-(4-Hydroxyphenyl)butylamidino-3,5-diamino-6-chloropyrazinecarboxamide hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cl.N=C(NCCCCc1ccc(O)cc1)NC(=O)c1nc(Cl)c(N)nc1N
Reaction #53374
5
収率 84.4%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N=C(NCCCc1ccc(O)cc1)NC(=O)c1nc(Cl)c(N)nc1N
Reaction #53377
compound 15
収率 60.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N=C(NCCCCCc1ccc(O)cc1)NC(=O)c1nc(Cl)c(N)nc1N
Reaction #53380
22
収率 131.5%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N=C(NCCCCc1ccc(O)c(O)c1)NC(=O)c1nc(Cl)c(N)nc1N
Reaction #53384
compound 28
収率 51.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N=C(NCCCCc1ccc(O)cc1O)NC(=O)c1nc(Cl)c(N)nc1N
Reaction #53391
81
収率 58.3%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OCC(COc2ccc(CCCCNC(=N)NC(=O)c3nc(Cl)c(N)nc3N)cc2)O1
Reaction #53401
Compound 37
収率 185.6%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N=C(NCCCCc1ccc(O)cc1)NC(=O)c1nc(Cl)c(N)nc1N
Reaction #53407
5
収率 84.4%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N=C(NCCCCc1ccc(CO)cc1)NC(=O)c1nc(Cl)c(N)nc1N
Reaction #53411
68
収率 194.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N=C(NCCc1ccc(N)cc1)N1C(N)=C(Cl)N=C(C(N)=O)C1N
Reaction #53414
83
収率 11.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N=C(NCCCCc1ccc(OCCN)cc1)NC(=O)c1nc(Cl)c(N)nc1N
Reaction #53421
4-[4-(2-aminoethyloxy)pheny)butylamidino-3,5-diamino-6-chloropyrazinecarboxamide hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(N)c(C(=O)NNC=NNC2=NCCS2)nc1Cl
Reaction #56265
3,5-diamino-6-chloro-N-{[(2-thiazolinylamino)iminomethyl]-amino}-2-pyrazinecarboxamide
DOI: 10.6084/m9.figshare.5104873.v1
Clc1nc2ccccc2nc1Nc1cccc2ccccc12
Reaction #72484
Compound 2c
収率 33.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cncc(-c2cc3c(cn2)cnn3-c2cnc(Cl)c(N3CCC[C@H](NC(=O)OC(C)(C)C)C3)n2)n1
Reaction #86214
desired product
収率 41.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cncc(-c2cc3c(cn2)cnn3-c2cnc(Cl)c(N3CCC[C@H](N)C3)n2)n1
Reaction #86215
226
収率 49.9%DOI: 10.6084/m9.figshare.5104873.v1
CS(C)=Nc1nccnc1Cl
Reaction #92887
2
収率 79.0%DOI: 10.6084/m9.figshare.5104873.v1
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