子结构搜索

16039

COc1ccc(-c2cc(C(=O)N[C@H]3CCCN(C(=O)OC(C)(C)C)C3)c(NC(N)=O)s2)cc1
Reaction #58613
light yellow solid
收率 67.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2cc(C(=O)N[C@H]3CCCNC3)c(NC(N)=O)s2)cc1
Reaction #58614
light yellow solid
收率 92.7%DOI: 10.6084/m9.figshare.5104873.v1
CNc1ccc(Oc2ccnc(NC(=O)C3CCN(C(=O)OC(C)(C)C)CC3)c2)cc1[N+](=O)[O-]
Reaction #59065
tert-butyl-4-(N-{4-[4-(methylamino)-3-nitrophenoxy]-2-pyridyl}carbamoyl)piperidinecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCCO[Si](C)(C)C(C)(C)C)C(=O)C1=Cc2ccc(-c3ccc(C(=O)N4CCCC4)cc3)cc2N=C(NC(=O)OC(C)(C)C)C1
Reaction #66269
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)C1=Cc2ccc(-c3ccc(C(=O)N(C)C)cc3)cc2N=C(NC(=O)OC(C)(C)C)C1
Reaction #66280
tert-butyl (1E,4E)-8-(4-(dimethylcarbamoyl)phenyl)-4-(dipropylcarbamoyl)-3H-benzo[b]azepin-2-ylcarbamate
收率 83.5%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)C1=Cc2ccc(-c3ccc(C(=O)N4CC[C@@H](O)C4)cc3)cc2N=C(NC(=O)OC(C)(C)C)C1
Reaction #66283
tert-butyl (1E,4E)-4-(dipropylcarbamoyl)-8-(4-((R)-3-hydroxypyrrolidine-1-carbonyl)phenyl)-3H-benzo[b]azepin-2-ylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)C1=Cc2ccc(-c3ccc(C(=O)N4C[C@H](O)[C@@H](O)C4)cc3)cc2N=C(NC(=O)OC(C)(C)C)C1
Reaction #66285
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(Cc1ccccc1O)C(=O)C1=Cc2ccc(-c3ccc(C(=O)N4CCCC4)cc3)cc2N=C(NC(=O)OC(C)(C)C)C1
Reaction #66295
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCCO)C(=O)C1=Cc2ccc(-c3ccc(C(=O)OCC)cc3)cc2N=C(N)C1
Reaction #66300
ethyl 4-((1E,4E)-2-amino-4-((3-hydroxypropyl)(propyl)carbamoyl)-3H-benzo[b]azepin-8-yl)benzoate
收率 35.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCCC(Nc2ccc(C#N)c(N)n2)C1
Reaction #85968
tert-Butyl 3-[(6-amino-5-cyanopyridin-2-yl)amino]piperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
Cl.N#Cc1ccc(NC2CCCNC2)nc1N
Reaction #85969
2-Amino-6-(piperidin-3-ylamino)pyridine-3-carbonitrile hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCCC(Nc2ccc([N+](=O)[O-])c(N)n2)C1
Reaction #85972
tert-Butyl 3-[(6-amino-5-nitropyridin-2-yl)amino]piperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Nc1nc(NC2CCCNC2)ccc1[N+](=O)[O-]
Reaction #85973
3-Nitro-N6-(piperidin-3-yl)pyridine-2,6-diamine hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CN(Cc2ccccc2)CC2(CCN(C(=O)OC(C)(C)C)CC2)O1
Reaction #160054
9-tert-butyl 2-methyl 4-benzyl-1-oxa-4,9-diazaspiro[5.5]undecane-2,9-dicarboxylate
收率 67.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CNCC2(CCN(C(=O)OC(C)(C)C)CC2)O1
Reaction #160055
9-tert-butyl 2-methyl 1-oxa-4,9-diazaspiro[5.5]undecane-2,9-dicarboxylate
收率 74.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CN(C(=O)c1nnn(-c2ccccc2F)c1CCc1nccs1)C1CC(C(=O)N2CCOCC2)CN(C(=O)OC(C)(C)C)C1
Reaction #173636
DOI: 10.1039/C8SC04228D
COCCCCn1c(C(=O)N(CC(C)C)C2CC(C(=O)N3CCCC3)CN(C(=O)OC(C)(C)C)C2)nc2cccc(F)c21
Reaction #181718
DOI: 10.1039/C8SC04228D
CC1CCc2ncnc(N3CC4(CCN(C(=O)OC(C)(C)C)CC4)c4c(CNc5ncccn5)cccc43)c21
Reaction #187895
DOI: 10.1039/C8SC04228D
Cc1c(N2CC(F)C(C3(NC(=O)OC(C)(C)C)CC3)C2)c(F)c(N)c2c(=O)c(C(=O)O)cn(C3CC3F)c12
Reaction #200213
DOI: 10.1039/C8SC04228D
O=C(Nc1ccc(Cl)cn1)c1cc(F)ccc1NCC1CCNCC1
Reaction #200390
DOI: 10.1039/C8SC04228D
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