部分構造検索

Cn1ccc2c(N)cccc21

CC(C)(C)OC(=O)Cn1cc2c3c(cccc31)NC(=O)CC2
Reaction #293655
DOI: 10.1039/C8SC04228D
O=C(O)Cn1cc2c3c(cccc31)NC(=O)CC2
Reaction #294091
DOI: 10.1039/C8SC04228D
COc1ccc(Cl)cc1NC(=O)Nc1cccc2c1ccn2Cc1ccnc2[nH]ccc12.Cl
Reaction #327654
1-(2-Methoxyl-5-chlorophenyl)-3-[1-(1H-pyrrolo[2,3-b]pyridin-4-ylmethyl)-1H-indol-4-yl]urea hydrochloride
収率 180.3%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cccc2c1ccn2Cc1ccnc2[nH]ccc12
Reaction #327655
4-[(4-nitro-1H-indol-1-yl)methyl]-1H-pyrrolo[2,3-b]pyridine
収率 16.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1ccc2c(Cn3ccc4c(N)cccc43)ccnc21
Reaction #327656
4-[(4-amino-1H-indol-1-yl)methyl]-1-(t-butyloxycarbonyl)-1H-pyrrolo[2,3-b]pyridine
収率 95.5%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #327657
1-(2-methoxyl-5-chlorophenyl)-3-{1-[1-(t-butyloxycarbonyl)-1H-pyrrolo[2, 3-1)]pyridin-4-ylmethyl]-1H-indol-4-yl
収率 80.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cl)cc1NC(=O)Nc1cccc2c1ccn2Cc1ccnc2[nH]ccc12.Cl
Reaction #327658
1-(2-Methoxyl-5-chlorophenyl)-3-[1-(1H-pyrrolo[2,3-b]pyridin-4-ylmethyl)-1H-indol-4-yl]urea hydrochloride
収率 180.3%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cccc2c1ccn2Cc1c[nH]c2ncccc12
Reaction #327659
3-[(4-nitro-1H-indol-1-yl)methyl]-1H-pyrrolo[2,3-b]pyridine
収率 34.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1cc(Cn2ccc3c(N)cccc32)c2cccnc21
Reaction #327660
3-[(4-amino-1H-indol-1-yl)methyl]-1-(t-butyloxycarbonyl)-1H-pyrrolo[2,3-b]pyridine
収率 99.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cl)cc1NC(=O)Nc1cccc2c1ccn2Cc1cn(C(=O)OC(C)(C)C)c2ncccc12
Reaction #327661
1-(2-methoxyl-5-chlorophenyl)-3-{1-[1-(t-butyloxycarbonyl)-1H-pyrrolo[2,3-b]pyridin-3-ylmethyl]-1H-indol-4-yl}urea
収率 73.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cl)cc1NC(=O)Nc1cccc2c1ccn2Cc1c[nH]c2ncccc12.Cl
Reaction #327662
1-(2-Methoxyl-5-chlorophenyl)-3-[1-(1H-pyrrolo[2,3-b]pyridin-3-ylmethyl)-1H-indol-4-yl]urea hydrochloride
収率 185.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc([N+](=O)[O-])c2ccn(C(C)C)c12
Reaction #328093
desired product
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(N)c2ccn(C(C)C)c12
Reaction #328094
desired product
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(N=C=S)c2ccn(C(C)C)c12
Reaction #328095
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2cccc3c2cc(C(=O)O)n3C)CC1
Reaction #376853
DOI: 10.1039/C8SC04228D
COc1ccc2c(c(C=O)cn2C)c1N
Reaction #398375
DOI: 10.1039/C8SC04228D
COC(=O)C=Cc1c(C(=O)OC)c2c([N+](=O)[O-])c(OC)ccc2n1C
Reaction #400262
DOI: 10.1039/C8SC04228D
CC1(C)C(C(=O)c2cn(CCN3CCOCC3)c3cccc(N)c23)C1(C)C
Reaction #400992
DOI: 10.1039/C8SC04228D
—
Reaction #419903
crude residue
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@@H](Nc1cnc(C(N)=O)c(Nc2cccc3c2ccn3C)n1)C(N)=O
Reaction #419904
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
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