부분 구조 검색

831552

CC(C)n1c(=O)n(C(=O)NCC2CCN(CC3(C(=O)O)CCOCC3)CC2)c2ccccc21.O=S(=O)(O)c1ccccc1
Reaction #44865
titled compound
수율 90.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCC1CCOCC1)c1cnc(N[C@@H]2C[C@H]3CC[C@@H]2C3)nc1C(F)(F)F
Reaction #67055
rac-2-[(1R,2R,4S)-bicyclo[2.2.1]hept-2-ylamino]-N-(tetrahydro-2H-pyran-4-ylmethyl)-4-(trifluoromethyl)pyrimidine-5-carboxamide
수율 87.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(N(C)CC2CCOCC2)c2sc(NC(=O)c3ccnc(Br)c3)nc12
Reaction #80171
2-bromo-N-{4-methoxy-7-[methyl-(tetrahydro-pyran-4-ylmethyl)-amino)-benzothiazol-2-yl}-isonicotinamide
수율 14.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN(Cc2ccc3c(c2)CC[C@H](N(C)C(=O)c2ccc(C4CCCCC4)cc2)C3)CC2CCOCC2)cc1
Reaction #164599
4-Cyclohexyl-N—((S)-6-{[(4-methoxybenzyl)(tetrahydropyran-4-ylmethyl)amino]methyl}-1,2,3,4-tetrahydronaphthalen-2-yl)-N-methylbenzamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CNCC2CCOCC2)cc1
Reaction #164601
(4-Methoxybenzyl)(tetrahydropyran-4-ylmethyl)amine
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN(Cc2ccc3c(c2)CC[C@H](N)C3)CC2CCOCC2)cc1
Reaction #164602
(S)-6-{[(4-Methoxybenzyl)(tetrahydropyran-4-ylmethyl)amino]methyl}-1,2,3,4-tetrahydronaphthalen-2-ylamine
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H](/C=C/C(=O)N1CCc2ccccc21)NC(=O)C1(NC(=O)OC(C)(C)C)CCOCC1
Reaction #165918
title compound
수율 38.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@@H](/C=C/C(=O)N1CCc2ccccc21)NC(=O)C1(NC(=O)OC(C)(C)C)CCOCC1
Reaction #165924
title compound
수율 31.3%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H](/C=C/C(=O)N1CCc2ccccc21)NC(=O)C1(N)CCOCC1.Cl
Reaction #165925
title compound
수율 89.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@@H](/C=C/C(=O)N1CCc2ccccc21)NC(=O)C1(N)CCOCC1.Cl
Reaction #165926
title compound
수율 60.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc2cc3c(cc2s1)C1(CO3)C(=O)N(CC2CCOCC2)c2ccccc21
Reaction #173892
DOI: 10.1039/C8SC04228D
Cc1nccn1-c1ccc(COc2cc(F)cc(C3(C(=O)N(C)C)CCOCC3)c2)cc1
Reaction #175981
DOI: 10.1039/C8SC04228D
N#Cc1ccc(N2C(=O)NC3(CCOCC3)C2=O)cc1C(F)(F)F
Reaction #179043
DOI: 10.1039/C8SC04228D
O=C(NCC1CCOCC1)c1ccc(S(=O)(=O)n2cc(C3CCCC3)c3ccccc32)cc1
Reaction #179118
DOI: 10.1039/C8SC04228D
CN(C(=O)c1ccc(Cl)cc1)C1CCN(C(=O)C2CCOCC2NC(=O)c2ccccc2)CC1c1ccc(Cl)c(Cl)c1
Reaction #181391
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC1(C(=O)NC(C#N)Cc2ccc(-c3ccc(S(=O)(=O)N4CCC4)cc3)cc2)CCOCC1
Reaction #190511
DOI: 10.1039/C8SC04228D
CN1C(=O)Cc2ccc(-c3ccc(CC(NC(=O)C4(NC(=O)OC(C)(C)C)CCOCC4)C(N)=O)cc3)cc21
Reaction #197080
DOI: 10.1039/C8SC04228D
CC(OC1OCC2CNCC2C1c1ccc(F)cc1)c1cc(C(F)(F)F)cc(C(F)(F)F)c1
Reaction #205690
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC1(C(=O)NC(Cc2ccc(-c3ccc(C#N)cc3)cc2)C(N)=O)CCOCC1
Reaction #209073
DOI: 10.1039/C8SC04228D
N#CC(Cc1ccc(-c2ccc(F)cc2)cc1)NC(=O)C1(N)CCOCC1
Reaction #229498
DOI: 10.1039/C8SC04228D
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