부분 구조 검색

413238

CCOC(=O)/C(F)=C/c1cnc(N[C@@H]2CCCNC2)c(Cl)c1.Cl.Cl
Reaction #313561
ethyl (2Z)-3-{5-chloro-6-[(3R)-3-piperidinylamino]-3-pyridinyl}-2-fluoroacrylate dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cnc(N[C@@H]2CCCN(C(=O)OC(C)(C)C)C2)c(Cl)c1
Reaction #313565
ethyl 6-{[(3R)-1-(tert-butoxycarbonyl)-3-piperidinyl]amino}-5-chloronicotinate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC[C@@H](Nc2ncc(C=O)cc2Cl)C1
Reaction #313566
tert-butyl (3R)-3-[(3-chloro-5-formyl-2-pyridinyl)amino]-1-piperidinecarboxylate
수율 91.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)/C(F)=C/c1cnc(N[C@@H]2CCCN(C(=O)OC(C)(C)C)C2)c(Cl)c1
Reaction #313567
tert-butyl (3R)-3-({3-chloro-5-[(1Z)-3-ethoxy-2-fluoro-3-oxo-1-propen-1-yl]-2-pyridinyl}amino)-1-piperidinecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(F)=Cc1cnc(NC2CCCN(C(=O)OC(C)(C)C)C2)c(Cl)c1
Reaction #392112
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC[C@@H](Nc2ncccc2Cl)C1
Reaction #675538
title compound
수율 73.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC[C@@H](N(C(=O)c2ccc(Br)cc2)c2ncccc2Cl)C1
Reaction #675547
title compound
수율 79.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC[C@@H](N(C(=O)c2ccc(Br)cc2)c2ncccc2Cl)C1
Reaction #675548
title compound
수율 63.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #675556
solid
수율 78.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC[C@@H](N(C(=O)c2ccc(-n3nnc4cccnc43)cn2)c2ncccc2Cl)C1
Reaction #675571
product
수율 52.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #675572
solid
수율 97.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cnc2c(c1)nnn2-c1ccc(C(=O)N(c2ncccc2Cl)[C@@H]2CCCN(C(=O)OC(C)(C)C)C2)nc1
Reaction #675574
product
수율 43.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC[C@@H](N(C(=O)c2ccc(-n3nnc4cccnc43)cc2)c2ncccc2Cl)C1
Reaction #675579
product
수율 79.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(F)=Cc1cnc(NC2CCCN(C(=O)OC(C)(C)C)C2)c(Cl)c1
Reaction #902523
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC[C@@H](N(C(=O)c2ccc(-c3cnn4cccnc34)cc2)c2ncccc2Cl)C1
Reaction #2102859
DOI: 10.1038/s41557
CC(C)(C)OC(=O)N1CCC[C@@H](N(C(=O)c2ccc(-c3cnn4cccnc34)cc2)c2ncccc2Cl)C1
Reaction #2102860
DOI: 10.1038/s41557
CC(C)(C)OC(=O)N1CCC[C@@H](N(C(=O)c2ccc(-c3cnn4cccnc34)cc2)c2ncccc2Cl)C1
Reaction #2102861
DOI: 10.1038/s41557
CC(C)(C)OC(=O)N1CCC[C@@H](N(C(=O)c2ccc(-c3cnn4cccnc34)cc2)c2ncccc2Cl)C1
Reaction #2102862
DOI: 10.1038/s41557
CC(C)(C)OC(=O)N1CCC[C@@H](N(C(=O)c2ccc(-c3cnn4cccnc34)cc2)c2ncccc2Cl)C1
Reaction #2102863
DOI: 10.1038/s41557
CC(C)(C)OC(=O)N1CCC[C@@H](N(C(=O)c2ccc(-c3cnn4cccnc34)cc2)c2ncccc2Cl)C1
Reaction #2102864
DOI: 10.1038/s41557
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