بحث البنية الفرعية

2493

CCCCS(=O)(=O)Nc1ccc(C(=O)N2Cc3cccn3Cc3ccccc32)cc1OC
Reaction #3711
light yellow solid
المردود 102.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOCc1nc2cnc3cc(Br)ccc3c2n1CCCCCS(=O)(=O)Cl
Reaction #9524
5-(7-bromo-2-ethoxymethyl-1H-imidazo[4,5-c]quinolin-1-yl)pentane-1-sulfonyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1c(-c2ccc(OS(=O)(=O)CC3CCCCC3)c3c2C(=O)NC3)cc2cc(CN3CCCCC3)ccc21
Reaction #49461
4-cyclohexylmethanesulfonyloxy-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone
المردود 80.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCS(=O)(=O)Nc1cc(-c2cc3cc(F)c(F)cc3[nH]2)ccc1OC
Reaction #53786
product
المردود 44.9%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCS(=O)(=O)Nc1cc(-c2nc3cc(Cl)c(Cl)cc3[nH]2)ccc1OC
Reaction #53789
product
المردود 4.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCC1(CF)OCCCO1)c1ccccc1
Reaction #59943
title compound
المردود 46.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C1NC(=O)C(CCOCc2ccccc2)(CS(=O)(=O)N2CCC(Oc3ccc(Cl)cn3)CC2)N1
Reaction #60673
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCS(=O)(=O)Nc1cnc2c(nc(CCC)n2Cc2ccc(-c3ccccc3S(N)(=O)=O)cc2)c1C
Reaction #64397
6-[(Butylsulfonyl)amino]-7-methyl-2-propyl-3-[2'-(aminosulfonyl)[1,1']-biphenyl-4-yl]methyl-3H-imidazo[4,5-b]pyridine
المردود 60.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncnc2c1c(-c1ccc(Oc3ccccc3)cc1)cn2S(=O)(=O)C1CCCC1
Reaction #79782
7-cyclopentanesulphonyl-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-4-ylamine
DOI: 10.6084/m9.figshare.5104873.v1
CCCCS(=O)(=O)Nc1ccc(C(=O)N2Cc3cccn3Cc3ccccc32)cc1OC
Reaction #83534
light yellow solid
المردود 102.9%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(NC1CCN(CCc2c[nH]c3ccccc23)CC1)C1CCCCC1
Reaction #94583
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCS(=O)(=O)Nc1ccc(F)c(F)c1Nc1ccc(I)cc1F
Reaction #160565
desired product
المردود 55.0%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(Nc1ccc(F)c(F)c1Nc1ccc(I)cc1F)C1CCCC1
Reaction #160569
desired product
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(Nc1ccc(F)c(F)c1Nc1ccc(I)cc1F)C1CCCCC1
Reaction #160570
desired product
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(F)c(F)c(Nc2ccc(I)cc2F)c1NS(=O)(=O)C1CCC1
Reaction #160611
title product
المردود 75.0%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(CC1CCCC1)N1CC(Nc2nc(-c3c[nH]c4ncc(Cl)cc34)ncc2F)C1
Reaction #162064
desired product
المردود 88.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCS(=O)(=O)N1CC[C@H](Nc2nc(-c3c[nH]c4ncc(Cl)cc34)ncc2F)C1
Reaction #162072
402
المردود 45.0%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(C1CCCC1)N1CC[C@H](Nc2nc(-c3c[nH]c4ncc(Cl)cc34)ncc2F)C1
Reaction #162073
403
المردود 20.0%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(CC1CCCC1)N1CC[C@H](Nc2nc(-c3c[nH]c4ncc(Cl)cc34)ncc2F)C1
Reaction #162075
479
المردود 58.0%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(C1CCCCC1)N1CCC(n2ncc(COc3ccc(-n4cnnn4)nc3)n2)CC1
Reaction #167839
title compound
DOI: 10.6084/m9.figshare.5104873.v1
الصفحة 1التالي