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21377

O=CCn1c(=O)cnc2ccc(Br)cc21
Reaction #68263
(7-bromo-2-oxoquinoxalin-1(2H)-yl)acetaldehyde
DOI: 10.6084/m9.figshare.5104873.v1
O=c1cnc2ccc(Br)cc2n1CCN1CCC(NCc2ccc3c(c2)OCCO3)CC1
Reaction #68264
1-(2-(4-((2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)piperidin-1-yl)ethyl)-7-bromoquinoxalin-2(1H)-one
収率 71.5%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=c1cnc2ccc(Br)cc2n1CCN1CCC(NCc2ccc3c(c2)OCCO3)CC1
Reaction #68265
1-(2-(4-((2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)piperidin-1-yl)ethyl)-7-bromoquinoxalin-2(1H)-one hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCc2c(c(Br)cc3[nH]c(=O)c(=O)[nH]c23)C1
Reaction #76485
title compound
収率 24.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1nc2cc(C)c3c(c2nc1OC)CCN(C)C3
Reaction #76521
title compound
収率 48.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(OCC)c1cc2nc(OCc3ccccc3)c(OCc3ccccc3)nc2c2c1CN(C)CC2
Reaction #76523
title compound
収率 36.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCc1ccccc1)C1Cc2cc(Br)cc3[nH]c(=O)c(=O)n1c23
Reaction #80745
title compound
収率 99.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCc1ccccc1)C1Cc2cc(Br)cc3[nH]c(=O)c(=O)n1c23
Reaction #80746
title compound
収率 96.3%DOI: 10.6084/m9.figshare.5104873.v1
Cl.NCC1Cc2cc(Br)cc3[nH]c(=O)c(=O)n1c23
Reaction #80748
title compound
収率 60.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CC1Cc2cc(Br)cc3[nH]c(=O)c(=O)n1c23)NCc1ccccc1
Reaction #80754
title compound
収率 51.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCC1Cc2cc(Br)cc3[nH]c(=O)c(=O)n1c23)c1ccccc1
Reaction #80755
title compound
収率 53.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccccc1)C1CCc2cc(Br)cc3[nH]c(=O)c(=O)n1c23
Reaction #80756
title compound
収率 84.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCc1ccccc1)C1CCc2cc(Br)cc3[nH]c(=O)c(=O)n1c23
Reaction #80757
title compound
収率 81.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCc1ccccc1)C1CCc2cc(Br)cc3[nH]c(=O)c(=O)n1c23
Reaction #80758
title compound
収率 84.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CC1CCc2cc(Br)cc3[nH]c(=O)c(=O)n1c23
Reaction #80762
title compound
収率 49.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCC1CCc2cc(Br)cc3[nH]c(=O)c(=O)n1c23)c1ccccc1
Reaction #80764
title compound
収率 59.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1CCCCC1)C1CCc2cc(Br)cc3[nH]c(=O)c(=O)n1c23
Reaction #80769
title compound
収率 91.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)OCC1CCc2cc(Br)cc3[nH]c(=O)c(=O)n1c23
Reaction #80770
title compound
収率 64.4%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c2cc(Br)cc3c2n(c1=O)C(CI)CC3
Reaction #80771
title compound
収率 78.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](Cc1ccccc1)NC(=O)C1CCc2cc(Br)cc3[nH]c(=O)c(=O)n1c23
Reaction #80772
title compound
収率 87.0%DOI: 10.6084/m9.figshare.5104873.v1
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