子结构搜索

24345

CC(C)[C@H](Nc1ncccn1)C(=O)N1CCC[C@H]1c1ncc(-c2ccc(-c3ccc(-c4cnc([C@@H]5CCCN5C(=O)OC(C)(C)C)[nH]4)cc3)cc2)[nH]1
Reaction #49155
title compound
收率 110.8%DOI: 10.6084/m9.figshare.5104873.v1
NCCCNc1ncccn1
Reaction #55131
2-(3-aminopropylamino)pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1
NCCCNc1ncccn1
Reaction #55800
2-(3-aminopropylamino)pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc([N+](=O)[O-])ccc1Oc1ncccn1
Reaction #66522
2-(2-methoxy-4-nitrophenoxy)pyrimidine
收率 78.0%DOI: 10.6084/m9.figshare.5104873.v1
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Reaction #70434
Example 48
收率 60.0%DOI: 10.6084/m9.figshare.5104873.v1
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Reaction #70435
Example 48
收率 64.0%DOI: 10.6084/m9.figshare.5104873.v1
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Reaction #70436
Example 48
收率 38.0%DOI: 10.6084/m9.figshare.5104873.v1
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Reaction #70437
Example 48
收率 73.0%DOI: 10.6084/m9.figshare.5104873.v1
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Reaction #70438
Example 48
收率 67.0%DOI: 10.6084/m9.figshare.5104873.v1
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Reaction #70439
Example 48
收率 65.0%DOI: 10.6084/m9.figshare.5104873.v1
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Reaction #70440
Example 48
收率 10.0%DOI: 10.6084/m9.figshare.5104873.v1
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Reaction #70441
Example 48
收率 45.0%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1cccc(-c2ncccn2)c1
Reaction #78837
title compound
收率 63.3%DOI: 10.6084/m9.figshare.5104873.v1
c1cnc(N2CCO[C@H](CNc3nc(-c4ccc(N5CCOCC5)cc4)cc4nccnc34)C2)nc1
Reaction #85925
(R)-7-(4-morpholinophenyl)-N-((4-(pyrimidin-2-yl)morpholin-2-yl)methyl)pyrido[4,3-b]pyrazin-5-amine
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)c2cc(Oc3ncccn3)ccc2C(=O)c2c1[nH]c1cc(C#N)ccc21
Reaction #89991
title compound
DOI: 10.6084/m9.figshare.5104873.v1
c1cnc(OCC2CCCCC2)nc1
Reaction #91629
2-(cyclohexylmethoxy)pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(OC)cccc1-c1ncccn1
Reaction #92482
title compound
收率 63.4%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c2ncccc2n1C1CCN(c2ccnc(Br)n2)CC1
Reaction #161796
1-[1-(2-bromo-pyrimidin-4-yl)-piperidin-4-yl]-1,3-dihydro-imidazo[4,5-b]-pyridin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
FC(F)Oc1ccc(Nc2ncc(Br)cn2)cc1Cl
Reaction #164663
5-bromo-N-(3-chloro-4-(difluoromethoxy)phenyl)pyrimidin-2-amine
收率 64.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@H](Nc1ncccn1)C(=O)N1CCC[C@H]1c1ncc(-c2ccc(-c3ccc(-c4cnc([C@@H]5CCCN5C(=O)OC(C)(C)C)[nH]4)cc3)cc2)[nH]1
Reaction #167561
title compound
收率 110.8%DOI: 10.6084/m9.figshare.5104873.v1
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