部分構造検索

325494

CCCCCCC(C)N(C(C)=O)c1ccc(I)cc1
Reaction #49638
N-acetyl-N-2-octyl-4-iodoaniline
収率 70.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCC(C)Nc1ccc(I)cc1
Reaction #49639
N-(4'-iodophenyl)-2-aminooctane
収率 88.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCC(C)N(C(C)=O)c1ccc(I)cc1
Reaction #49708
N-acetyl-N-2-octyl-4-iodoaniline
収率 70.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCC(C)Nc1ccc(I)cc1
Reaction #49709
N-(4'-iodophenyl)-2-aminooctane
収率 88.0%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(NC23CC4CC(CC(C4)C2)C3)cc1
Reaction #69933
desired product
収率 65.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CCCc2c(Cc3ccccc3)c3cccc(OC)c3n21
Reaction #79744
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(CN2CC3(Nc4ccc5[nH]ncc5c4)CCC2CC3)cc1
Reaction #162884
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(CN2CC3(Nc4ccc5[nH]ncc5c4)CCC2CC3)cc1OCCO
Reaction #162885
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(CN2CC3(Nc4ccc5[nH]ncc5c4)CCC2CC3)c1
Reaction #162886
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Nc2cc(N[C@H](CC3CCCCC3)C(N)=O)ccc2C#N)sn1
Reaction #172007
(R)-2-(4-cyano-3-(3-methylisothiazol-5-ylamino)phenylamino)-3-cyclohexylpropanamide
収率 99.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Nc2cc(N[C@H](CC3CCCCC3)C(N)=O)ccc2C(N)=O)sn1
Reaction #172008
titled compound
収率 32.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(=O)N2c3ccccc3C(n3c4ccccc4c4ccccc43)CC2CCCCCN2CCC(c3cccc(C(F)(F)F)c3)CC2)cc1OC
Reaction #178307
DOI: 10.1039/C8SC04228D
Cc1c(C(Nc2ccc(C(=O)N(C)CCC(=O)O)cc2)C2CCCCC2)oc2ccc(OCc3ccccc3)cc12
Reaction #179329
DOI: 10.1039/C8SC04228D
CCOC(=O)CCN(C)C(=O)c1ccc(NC(c2oc3ccc(-c4ccc(OC)nc4)cc3c2C)C2CCCCC2)cc1
Reaction #186418
DOI: 10.1039/C8SC04228D
COc1ccc2c(C(Nc3ccc(C(=O)N(C)CCC(=O)O)cc3)C3CCCCC3)c(C)oc2c1
Reaction #191384
DOI: 10.1039/C8SC04228D
CCCCCCN(C)C(=O)CCCCC1CC(n2c3ccccc3c3ccccc32)c2ccccc2N1C(=O)c1ccc(OC)c(OC)c1
Reaction #194029
DOI: 10.1039/C8SC04228D
CCOC(=O)CCN(C)C(=O)c1ccc(NC(c2oc3cc(F)ccc3c2C)C2CCCCC2)cc1
Reaction #197754
DOI: 10.1039/C8SC04228D
CCOC(=O)CCNC(=O)CCCCC1CC(n2c3ccccc3c3ccccc32)c2ccccc2N1C(=O)c1ccc(OC)c(OC)c1
Reaction #201682
DOI: 10.1039/C8SC04228D
Cc1c(C(Nc2ccc(C(=O)O)cc2)C2CCCC2)oc2ccc(F)cc12
Reaction #202968
DOI: 10.1039/C8SC04228D
COCc1c(C(Nc2ccc(C(=O)N(C)CCC(=O)O)cc2)C2CCCCC2)oc2ccc(F)cc12
Reaction #207229
DOI: 10.1039/C8SC04228D
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