部分構造検索

CC(C)N1CCNCC1

CNC(=O)C(Cc1ccc2ccccc2c1)N1CCNC(CCO[Si](C)(C)C(C)(C)C)C1=O
Reaction #8626
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CC2CC1CN2c1cnc(-c2nn(Cc3ccccc3F)c3ncccc23)nc1
Reaction #8682
1-(2-Fluorobenzyl)-3-[5-(5-isopropyl-2,5-diazabicyclo[2.2.1]hept-2-yl)-2-pyrimidinyl]-1H-pyrazol[3,4-b]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(N2CCN(C3CCCC3)CC2)cc1
Reaction #10887
1-cyclopentyl-4-(4-nitrophenyl)piperazine
DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2CCC1CN1CCN(C(c2ccccc2)c2ccccc2)CC1
Reaction #54469
2-(4-benzhydryl-1-piperazinylmethyl)-3,4-dihydro-1(2H)-naphthalenone
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)CCC(CN1CCN(C(c3ccccc3)c3ccccc3)CC1)C2O
Reaction #54470
2-(4-benzhydryl-1-piperazinylmethyl)-6-methoxy-1,2,3,4-tetrahydro-1-naphthalenol
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)N1CCN(c2ccc([N+](=O)[O-])cc2)CC1
Reaction #72917
title compound
収率 272.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)N1CCN(c2ccc(N)cc2)CC1
Reaction #72918
amine
収率 89.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1N1CCN(C2CC=C(c3c(C)ccnc3C)CC2)CC1
Reaction #82482
title product
収率 74.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1N1CCN(C2CC=C(c3ncc(C)cc3C)CC2)CC1
Reaction #82483
title compound
収率 61.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCN(c2ccc(NC(=O)OC(C)(C)C)c([N+](=O)[O-])c2)CC1
Reaction #86471
title compound
収率 70.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCN(c2ccc(N)c([N+](=O)[O-])c2)CC1
Reaction #86472
title compound
収率 115.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cnc2cc(OCCN3CCN(C(C)C)CC3)ccn12
Reaction #166572
ethyl 7-(2-(4-isopropylpiperazin-1-yl)ethoxy)imidazo[1,2-a]pyridine-3-carboxylate
収率 59.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCN(CCOc2ccn3c(C(=O)[O-])cnc3c2)CC1.[Li+]
Reaction #166573
product
収率 101.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCN(CCOc2ccn3c(C(=O)Nc4cccc5c4c(C4CC4)nn5Cc4ccn(C(C)C)n4)cnc3c2)CC1
Reaction #166581
product
収率 61.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCN(C(=O)c2ccc3c(c2)cc(C(=O)N2CCS(=O)(=O)CC2)n3CC#N)CC1
Reaction #173454
DOI: 10.1039/C8SC04228D
CC1(CN2CCN(C3CCN(c4ccc(OC(F)(F)F)cc4)CC3)CC2)Cn2cc([N+](=O)[O-])nc2O1
Reaction #179665
DOI: 10.1039/C8SC04228D
CCC(CC)C(=O)Nc1ccc(N2CCN(C(C(=O)N(CC)CC)c3ccccc3)CC2)c(C#C[Si](C)(C)C)c1
Reaction #183673
DOI: 10.1039/C8SC04228D
CC(C)N1CCN(C(=O)c2ccc3[nH]c(C(=O)N4CCN(S(=O)(=O)N5CCCCC5)CC4)cc3c2)CC1
Reaction #185009
DOI: 10.1039/C8SC04228D
CC(C)N1CCN(C(=O)c2ccc3c(c2)cc(C(=O)N2CCN(C(=O)C4CC4)CC2)n3-c2ccc(Cl)nc2)CC1
Reaction #187101
DOI: 10.1039/C8SC04228D
O=C(c1ccc2[nH]c(C(=O)N3CCOCC3)cc2c1)N1CCN(C2CCCC2)CC1
Reaction #192711
DOI: 10.1039/C8SC04228D
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