部分構造検索

917566

COc1cccc(-c2ccc3c(c2)C(C)(C)C(=O)N3)c1
Reaction #9420
5-(3-methoxy-phenyl)-3,3-dimethyl-1,3-dihydro-indol-2-one
収率 31.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(Br)c(-c2ccccc2)c(C)c(C#N)c1NC(=O)C(F)(F)F
Reaction #45573
compound
収率 84.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(N)c(C#N)c(C)c(-c2ccccc2)c1Br
Reaction #45575
compound
収率 94.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(N)c(C#N)c(C)c(-c2cccc(OCc3ccccc3)c2)c1F
Reaction #45588
compound
収率 87.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2)c(F)c2oc(C(C)(C)COCc3ccccc3)nc2c1C#N
Reaction #45595
compound
収率 90.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(Cl)c(-c2ccc(C(=O)O)c3ncc(N(C)CCN(C)C)nc23)c1Cl
Reaction #71386
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(F)c(-c2ccc(C(=O)Nc3cccnc3)c3nccnc23)c1F
Reaction #71396
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(Cl)c(-c2ccc(C(=O)Nc3nc(CN4CCN(C)CC4)c[nH]3)c3nccnc23)c1F
Reaction #71465
Title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(Cl)c(-c2ccc(C(=O)Nc3nc(CN4CCNC(=O)C4)c[nH]3)c3nccnc23)c1F
Reaction #71466
Title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(Cl)c(-c2ccc3nc(N[C@@H]4[C@H]5C[C@H]5C[C@@H]4NC(=O)OCC[Si](C)(C)C)ncc3c2)c1Cl
Reaction #84649
title compound
収率 62.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(Cl)c(-c2ccc3nc(N[C@@H]4[C@H]5C[C@H]5C[C@@H]4N)ncc3c2)c1Cl
Reaction #84650
title compound
収率 46.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(Cl)c(-c2ccc3nc(N[C@@H]4COCC[C@@H]4N)ncc3c2)c1Cl
Reaction #84658
(3S,4S)—N3-(6-(2,6-dichloro-3,5-dimethoxyphenyl)quinazolin-2-yl)tetrahydro-2H-pyran-3,4-diamine
収率 101.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CC(=O)N[C@H]1CCOC[C@H]1Nc1ncc2cc(-c3c(Cl)c(OC)cc(OC)c3Cl)ccc2n1
Reaction #84659
N-((3S,4S)-3-((6-(2,6-dichloro-3,5-dimethoxyphenyl)quinazolin-2-yl)amino)tetrahydro-2H-pyran-4-yl)acrylamide
収率 61.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Br)c(-c2c(C(C)C)cc(C(C)C)cc2C(C)C)cc1OC
Reaction #166156
title compound
収率 32.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(F)c(-c2ccc(CO)cc2C2=CCCC2(C)C)c1
Reaction #175749
DOI: 10.1039/C8SC04228D
COc1ccc(F)c(-c2ccc(CO[Si](C)(C)C(C)(C)C)cc2C(O)C(C)(C)C)c1
Reaction #182519
DOI: 10.1039/C8SC04228D
COc1c(Br)c(-c2ccccc2)c(C)c(C#N)c1NC(=O)C(F)(F)F
Reaction #183445
DOI: 10.1039/C8SC04228D
COc1ccc(F)c(-c2ccc(CO)cc2C(C)C(C)C)c1
Reaction #190491
DOI: 10.1039/C8SC04228D
COc1cc(OC)c(Cl)c(-c2ccc(C(=O)O)c3ncc(N(C)CCN(C)C)nc23)c1Cl
Reaction #191737
DOI: 10.1039/C8SC04228D
O=C(c1ccc(-c2ccc3c(c2)OCCO3)cc1F)N1CCCC1CN1CCCC1
Reaction #196224
DOI: 10.1039/C8SC04228D
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