Recherche de Sous-structure

862010

CCCCN1CCC(CC2CCCC3c4ccccc4N(C(=O)O)C23)CC1
Reaction #1712
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C#CCNC(=O)N1c2ccccc2C(=O)Nc2cccnc21
Reaction #4264
5,11-Dihydro-11-[[(2-propynyl)-amino]carbonyl]-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one
DOI: 10.6084/m9.figshare.5104873.v1
C#CCN(C)C(=O)N1c2ccccc2C(=O)Nc2cccnc21
Reaction #4265
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
C#CCOC(=O)N1c2ccccc2C(=O)Nc2cccnc21
Reaction #4266
5,11-Dihydro-11-[[(2-propynyl)oxy]carbonyl]-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one
DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)N1CCNCC1)c1ccccc1.Cl
Reaction #51236
1-(N-methyl-N-phenylaminocarbonyl)piperazine.hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(C)c1N(C)C(=O)Cl
Reaction #54295
2,6-dimethylphenyl-N-methylcarbamoyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=N)NC(=O)N(C)c1c(C)cccc1C.O=[N+]([O-])O
Reaction #54296
1-(2',6'-dimethylphenyl)-1-methyl-3-methylamidinourea nitrate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCN(C(=O)Cl)c1c(C)cccc1C
Reaction #54298
2,6-dimethyl-N-butylphenylcarbamoyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(C(=O)Cl)c1c(C)cccc1C
Reaction #54299
2,6-dimethyl-N-pentylphenylcarbamoyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1CC1)N(c1ccccc1)c1ccccc1
Reaction #56311
1-cyclopropyl-3,3-diphenylurea
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #69623
resultant compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)N1CCN(c2ccc(N3CCN(C(=O)Cl)c4ccccc43)nc2)CC1
Reaction #70252
4-[5-(4-tert-butyl-piperazin-1-yl)pyridin-2-yl]-3,4-dihydro-2H-quinoxaline-1-carbonyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)O[C@]1(C(=O)C(O)OC(=O)[C@@H](NC(=O)[C@@H]2CCCN2C(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)N(c2ccccc2)c2ccccc2)C(C)C)CC[C@H]2[C@@H]3C[C@H](C)C4=CC(=O)C=C[C@]4(C)[C@H]3[C@@H](O)C[C@@]21C
Reaction #81340
N-(N -(N-(N-(diphenylcarbamoyl)-L-alanyl)-L-alanyl)-L-prolyl)-L-valine [11β,21-dihydroxy-3,20-dioxo-6α-methyl-17-propionyloxy-pregna -1,4-dien-21-yl] ester
Rendement 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CSCO[C@H]1C[C@H](n2cnc3c(OC(=O)N(c4ccccc4)c4ccccc4)nc(NC(=O)C(C)C)nc32)O[C@@H]1CO[Si](C)(C)C(C)(C)C
Reaction #86790
product 12
Rendement 80.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(OC(=O)N(c2ccccc2)c2ccccc2)nc(C(Cl)(Cl)Cl)n1
Reaction #94996
residue
Rendement 88.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)N1CCNCC1)c1ccccc1
Reaction #173840
DOI: 10.1039/C8SC04228D
CN(C(=O)Oc1ncc(Oc2ccc(Cl)c(Cl)c2)cn1)c1ccccc1
Reaction #174194
DOI: 10.1039/C8SC04228D
CC(=O)c1cnn(OC(=O)N(C)c2ccccc2)c1
Reaction #175243
DOI: 10.1039/C8SC04228D
COc1ccc(-c2ccn(OC(=O)N(C)c3ccccc3)n2)cc1
Reaction #176263
DOI: 10.1039/C8SC04228D
CN1CCC(c2c[nH]c3ccc(NC(=O)N(C)c4ccccc4)cc23)CC1
Reaction #176466
DOI: 10.1039/C8SC04228D
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