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847451

CNC(=O)C(Cc1ccc2ccccc2c1)N1CCN(C(=O)OC(C)(C)C)C(CCOC(C)=O)C1
Reaction #8628
desired product
DOI: 10.6084/m9.figshare.5104873.v1
COC(CCCN1CCN(C(=O)OC(C)(C)C)CCC1=O)OC
Reaction #10277
4-(4,4-dimethoxybutyl)-5-oxo-[1,4]diazepane-1-carboxylic acid tert-butyl ester
Выход 51.8%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)[C@H]1CN(C(=O)OC(C)(C)C)C[C@@H]1O
Reaction #42054
(3S,4S)-1-(t-butoxycarbonyl)-3-(dimethylamino)-4-hydroxypyrrolidine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(Cc2cccc(-c3ccnc(Cl)n3)c2)CC1Cc1ccccc1
Reaction #43165
2-Benzyl-4-[3-(2-chloro-pyrimidin-4-yl)-benzyl]-piperazine-1-carboxylic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
Oc1ccc(CCNc2nccc(-c3cccc(CN4CCN[C@H](Cc5ccccc5)C4)c3)n2)cc1
Reaction #43166
4-(2-{4-[3-(3(R)-Benzyl-piperazin-1-ylmethyl)-phenyl]-pyrimidin-2-ylamino}-ethyl)-phenol
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(Cc2cccc(-c3ccnc(Cl)n3)c2)C[C@H]1c1ccccc1
Reaction #43184
(2R)-tert-butyl 4-(3-(2-chloropyrimidin-4-yl)benzyl)-2-phenylpiperazine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(CO)N1CCN(C(=O)OC(C)(C)C)CC1
Reaction #45117
tert-butyl 4-(1-hydroxypropan-2-yl)piperazine-1-carboxylate
Выход 33.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(CO)N1CCNCC1
Reaction #45118
2-(piperazin-1-yl)propan-1-ol
Выход 113.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N(CCC#N)CC(=O)NCCc1ccc2c(c1)OCO2
Reaction #51479
2-[(2-cyanoethyl)(dimethylethoxycarbonyl)amino]-N-[2-(1,3-benzodioxol-5-yl)ethyl]acetamide
Выход 88.8%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=O)CN(C(=O)OC(C)(C)C)[C@@H]2C[C@H]2c2ccc(-c3ccccc3)cc2)CC1
Reaction #66395
tert-butyl (trans)-2-(1,1′-biphenyl-4-yl)cyclopropyl(2-(4-methylpiperazin-1-yl)-2-oxoethyl)carbamate
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=O)CN[C@@H]2C[C@H]2c2ccc(-c3ccccc3)cc2)CC1
Reaction #66396
2-((trans)-2-(1,1′-biphenyl-4-yl)cyclopropylamino)-1-(4-methylpiperazin-1-yl)ethanone
Выход 15.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H]1CNCCN1C(=O)OC(C)(C)C
Reaction #66555
sub-title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@@H]2CCN(C(=O)OC(C)(C)C)C[C@H]2NC(=O)OCc2ccccc2)nc1Cl
Reaction #71816
title compound
Выход 69.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1sc(N2CC[C@@H](NC(=O)c3nc(Cl)c(CC)[nH]3)[C@H](NC(=O)OCc3ccccc3)C2)nc1C
Reaction #71817
title compound
Выход 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1sc(N2C[C@@H]3[C@H]2CCN3C(=O)OC(C)(C)C)nc1C
Reaction #72201
title compound
Выход 99.5%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=O)OC(C)(C)C)C[C@@H]1CO
Reaction #88528
(R)-tert-butyl 3-(hydroxymethyl)-4-methylpiperazine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CSc1nn(-c2ccccc2)c2cc(N3CC(N4CCN(C(=O)OC(C)(C)C)CC4)C3)ccc12
Reaction #155866
tert-butyl 4-(1-(3-(methylthio)-1-phenyl-1H-indazol-6-yl)azetidin-3-yl)piperazine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COc1nn(-c2ccccc2)c2cc(N3CC(N4CCNCC4)C3)ccc12.Cl
Reaction #155889
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CNCCN(CCCOc1ccc2c(ccc(=O)n2C)c1)Cc1ccncc1.Cl.Cl.Cl
Reaction #156214
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CNCCN(CCCOc1ccc2c(ccc(=O)n2C)c1)Cc1ccncc1
Reaction #156215
title compound
Выход 109.4%DOI: 10.6084/m9.figshare.5104873.v1
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