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CNCCOC

CC(C)NC(=O)NS(=O)(=O)c1cc(Cl)ccc1OCC(=O)N1C[C@H](C)N(Cc2ccc(F)cc2)C[C@H]1C
Reaction #11760
title compound
収率 72.1%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)COc1ccc(Cl)cc1S(=O)(=O)NC(=O)C(C)(C)C
Reaction #11761
title compound
収率 49.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CN1C(=O)CN(CC(=O)OC)C1=NN=Cc1ccccc1
Reaction #49686
2-benzylidenehydrazono-3-ethoxycarbonylmethyl-1-methoxycarbonylmethylimidazolidin-4-one
収率 44.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CN1C(=O)CN2CC(=O)NN=C21
Reaction #49687
7-ethoxycarbonylmethyl-1,4,5,7-tetraazabicyclo[4,3,0]-nonan-5-ene-3,8-dione
収率 39.1%DOI: 10.6084/m9.figshare.5104873.v1
C=CCN1N=C(c2ccc3c(c2)N(S(C)(=O)=O)CCO3)CCC1=O
Reaction #63460
6-(3,4-Dihydro-4-methanesulfonyl-1,4(2H)-benzoxazin-6-yl)-2,3,4,5-tetrahydro-2-(2-propenyl)pyridazin-3-one
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(=O)N2CCOc3ccc(C4=NNC(=O)CC4)cc32)cc1OC
Reaction #63461
6-(3,4-Dihydro-4-(3,4-dimethoxyphenylcarbonyl)-1,4(2H)-benzoxazin-6-yl)-2,3,4,5-tetrahydropyridazin-3-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CNC[C@@H]1COc2ccc(S(C)(=O)=O)cc2O1
Reaction #67183
2-METHYL-N-{[(2R)-7-(METHYLSULFONYL)-2,3-DIHYDRO-1,4-BENZODIOXIN-2-YL]METHYL}PROPAN-1-AMINE
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CNC[C@H]1COc2ccc(S(C)(=O)=O)cc2O1
Reaction #67184
2-METHYL-N-{[(2S)-7-(METHYLSULFONYL)-2,3-DIHYDRO-1,4-BENZODIOXIN-2-YL]METHYL}PROPAN-1-AMINE
DOI: 10.6084/m9.figshare.5104873.v1
COCCNCC1COc2ccc(S(C)(=O)=O)cc2O1
Reaction #67199
2-METHOXY-N-{[7-(METHYLSULFONYL)-2,3-DIHYDRO-1,4-BENZODIOXIN-2-YL]METHYL}ETHANAMINE
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CNCC1COc2ccc(S(C)(=O)=O)cc2O1
Reaction #67200
2-METHYL-N-{[7-(METHYLSULFONYL)-2,3-DIHYDRO-1,4-BENZODIOXIN-2-YL]METHYL}PROPAN-1-AMINE
DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@H]2CCN(c3cccc(C(=O)OC)n3)C[C@H]2OC)nc1Cl
Reaction #72027
title compound
収率 120.9%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)CN1C(=O)C(N)C(c2cccs2)Sc2ccccc21
Reaction #176986
DOI: 10.1039/C8SC04228D
CCOC(CN1CCN(S(=O)(=O)c2ccc3ncnc(Cl)c3c2)CC1)c1ccccc1
Reaction #180839
DOI: 10.1039/C8SC04228D
COc1ccccc1NC(=O)CC(=O)Nc1ccc(Oc2ccnc3cc(-c4cnc(=O)n(CCN5CCOCC5)c4)sc23)c(F)c1
Reaction #185033
DOI: 10.1039/C8SC04228D
CC(C)(O)c1cc(F)c(-c2nc(C(N)=O)c(Nc3cccc(C(CO)N4CCOCC4)n3)s2)c(F)c1
Reaction #189980
DOI: 10.1039/C8SC04228D
CN(C(=O)NCc1cccc(F)c1Cl)C(CCC(=O)N1CCNCC1)COC(=O)Nc1cc2ccccc2cn1
Reaction #193492
DOI: 10.1039/C8SC04228D
COc1ccc(S(=O)(=O)N2CCCC(NC(=O)C(CC(C)C)NC(=O)COCc3ccccc3)C(=O)C2)cc1
Reaction #200527
DOI: 10.1039/C8SC04228D
C#CCC(NS(=O)(=O)c1ccc(C)cc1)C(=O)NCC(OC)OC
Reaction #200597
DOI: 10.1039/C8SC04228D
O=S(=O)(NCCN1CCOCC1)c1ccc(Br)cc1
Reaction #208396
DOI: 10.1039/C8SC04228D
CN1CCN(CCCC(COC(=O)Nc2cc3ccccc3cn2)N(C)C(=O)NCc2cccc(F)c2Cl)CC1
Reaction #212335
DOI: 10.1039/C8SC04228D
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