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1336384

O=C(N[C@@H](Cc1ccc([N+](=O)[O-])cc1)C(=O)O)c1c(Cl)cccc1Cl
Reaction #45198
Nα-(2,6-dichlorobenzoyl)-4-nitro-L-phenylalanine
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H](Cc1ccc([N+](=O)[O-])cc1)C(=O)O)c1c(Cl)cccc1Cl
Reaction #45200
Nα-(2,6-dichlorobenzoyl)-4-nitro-L-phenylalanine
Выход 97.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1n[nH]cc1NC(=O)c1c(Cl)cccc1Cl
Reaction #48603
4-(2,6-dichloro-benzoylamino)-1H-pyrazole-3-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H](Cc1ccc(O)cc1)NC(=O)c1c(Cl)cccc1Cl
Reaction #52907
N-(2,6-dichlorobenzoyl)-D-tyrosine methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #56963
solid
Выход 25.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCS(=O)(=O)Nc1ccc(F)c(C(=O)c2cn(C(=O)c3c(Cl)cccc3Cl)c3ncc(Br)cc23)c1F
Reaction #88363
desired compound
Выход 36.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCS(=O)(=O)Nc1ccc(F)c(C(=O)c2cn(C(=O)c3c(Cl)cccc3Cl)c3ncc(B4OC(C)(C)C(C)(C)O4)cc23)c1F
Reaction #88382
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](Cc1ccc(NC(=O)c2c(Cl)cccc2Cl)cc1)NC(=O)OC(C)(C)C
Reaction #91994
(S)-2-tert-butoxycarbonylamino-3-[4-(2,6-dichlorobenzoylamino)phenyl]propionic acid methyl ester
Выход 88.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1nc(C(Cl)(Cl)Cl)ns1)c1c(Cl)cccc1Cl
Reaction #95222
pure product
Выход 22.0%DOI: 10.6084/m9.figshare.5104873.v1
COCCn1c(C)c(C)s/c1=N\C(=O)c1c(Cl)cccc1Cl
Reaction #165620
title compound
Выход 30.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccn2c(C(=O)Nc3cccc4c3c(CC)nn4Cc3cccc(C)n3)cnc2c1
Reaction #166501
final product
Выход 82.5%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nn(Cc2cc(C)n(C)n2)c2cccc(NC(=O)c3cnc4ccccn34)c12
Reaction #166556
final product
Выход 45.5%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nn(Cc2cc(C)n(C)n2)c2cccc(NC(=O)c3cnc4cc(OCCN5CCN(C)CC5)ccn34)c12
Reaction #166558
final product
Выход 68.7%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nn(Cc2ccn(C)n2)c2cccc(NC(=O)c3cnc4ccccn34)c12
Reaction #166562
final product
Выход 66.4%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nn(Cc2ccn(C)n2)c2cccc(NC(=O)c3cnc4cc(OCCN5CCN(C)CC5)ccn34)c12
Reaction #166563
final product
Выход 66.9%DOI: 10.6084/m9.figshare.5104873.v1
CCn1ccc(Cn2nc(C3CC3)c3c(NC(=O)c4cnc5cc(OCCN6CCN(C)CC6)ccn45)cccc32)n1
Reaction #166571
final product
Выход 66.8%DOI: 10.6084/m9.figshare.5104873.v1
CCn1ccc(Cn2nc(C3CC3)c3c(NC(=O)c4cnc5cc(OCCN6CCN(C(C)C)CC6)ccn45)cccc32)n1
Reaction #166574
final product
Выход 75.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)n1ccc(Cn2nc(C3CC3)c3c(NC(=O)c4cnc5cc(OCCN6CCN(C)CC6)ccn45)cccc32)n1
Reaction #166580
final product
Выход 70.5%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
Выход 61.1%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nn(Cc2cccc(C)n2)c2cccc(NC(=O)c3c(C#N)nc4ccccn34)c12
Reaction #166599
cyano-N-(3-ethyl-1-((6-methylpyridin-2-yl)methyl)-1H-indazol-4-yl)imidazo[1,2-a]pyridine-3-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
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