dimethoxyethane water

COc1ccc(-c2cc(-c3nc4ccccc4o3)ccc2CC#N)c(OC)c1
Reaction #7781
[5-(1,3-benzoxazol-2-yl)-2′,4′-dimethoxy-1,1′-biphenyl-2-yl]acetonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1cc(-c2nc3ccccc3o2)ccc1CC#N
Reaction #7782
[4-(1,3-benzoxazol-2-yl)-2-methylphenyl]acetonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1ccc(-c2nc3ccccc3o2)cc1-c1cccc(C#N)c1
Reaction #7785
5′-(1,3-benzoxazol-2-yl)-2′-methyl-1,1′-biphenyl-3-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(c1ccccc1)n1c(=O)c(-c2cccnc2)cn(CCCCl)c1=O
Reaction #40952
title compound
Yield 20.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1cc(-c2cn(CCCCCl)c(=O)n(C(=O)c3ccccc3)c2=O)ccn1
Reaction #40955
title compound
Yield 25.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1ncccc1-c1cn(CCCCCl)c(=O)n(C(=O)c2ccccc2)c1=O
Reaction #40957
title compound
Yield 66.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(c1ccccc1)n1c(=O)c(-c2cccnc2F)cn(CCCCCl)c1=O
Reaction #41027
title compound
Yield 54.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=c1[nH]c(=O)n(CCCN2C[C@@H]3C[C@]3(c3ccc(C(F)(F)F)cc3)C2)cc1-c1ccccc1F
Reaction #41045
title compound
Yield 76.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=c1[nH]c(=O)n(CCCN2C[C@@H]3C[C@]3(c3ccc(C(F)(F)F)cc3)C2)cc1-c1ccncc1
Reaction #41048
title compound
Yield 32.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=[N+]([O-])Nc1ccccc1
Reaction #41786
desired product 7
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cn1cc(-c2cnc3nnn(Cc4ccc5c(c4)CCO5)c3n2)cn1
Reaction #44272
1-(2,3-dihydro-benzofuran-5-ylmethyl)-6-(1-methyl-1H-pyrazol-4-yl)-1H-[1,2,3]triazolo[4,5-b]pyrazine
Yield 24.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)[C@H](Cc1ccc(-c2c(C#N)cccc2C(N)=O)cc1)NC(=O)c1c(Cl)cccc1Cl
Reaction #52936
N-(2,6-dichlorobenzoyl)-4-(2-cyano-6-carbamoyl-phenyl)-L-phenylalanine methyl ester
Yield 65.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCOC(=O)[C@H](Cc1ccc(-c2c(OC)cc(CO[Si](c3ccccc3)(c3ccccc3)C(C)(C)C)cc2OC)cc1)NC(=O)c1c(Cl)cccc1Cl
Reaction #52954
N-(2,6-dichlorobenzoyl)-4-[2,6-dimethoxy-4-[(t-butyldiphenylsilyloxy)methyl]phenyl]-L-phenylalanine ethyl ester
Yield 97.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCOC(=O)[C@H](Cc1ccc(-c2c(OC)cc(CN3CCSCC3)cc2OC)cc1)NC(=O)c1c(Cl)cccc1Cl
Reaction #52955
N-(2,6-dichlorobenzoyl)-4-[2,6-dimethoxy-4-(thiomorpholinomethyl)phenyl]-L-phenylalanine ethyl ester
Yield 15.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCOC(=O)[C@H](Cc1ccc(-c2c(OC)cc(O)cc2OC)cc1)NC(=O)c1c(Cl)cccc1Cl
Reaction #52971
N-(2,6-dichlorobenzoyl)-4-(2,6-dimethoxy-4-hydroxyphenyl)-L-phenylalanine ethyl ester
Yield 53.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
O=[N+]([O-])c1ccc(Cl)c(-c2ccncc2F)c1
Reaction #59077
4-(2-chloro-5-nitrophenyl)-3-fluoropyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COC1CCN(c2ccc([N+](=O)[O-])c(C3=CC(C)(C)CC(C)(C)C3)c2)CC1
Reaction #60426
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC[C@@H]1C(=O)N(C)c2cnc(-n3ccnc3-c3ccc(S(C)(=O)=O)cc3)nc2N1C1CCCC1
Reaction #73125
title compound
Yield 2.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
N#Cc1ccc(-c2ccccc2)cc1N
Reaction #77697
desired compound
Yield 91.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COc1ccc(C(c2ccc(OC)cc2)(c2ccc(OC)cc2)n2cc(-c3ccc(C=O)cc3)cn2)cc1
Reaction #84789
4-(1-(tris(4-methoxyphenyl)methyl)-1H-pyrazol-4-yl)benzaldehyde
Yield 83.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
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