CHCl3 H2O

CCCC(c1cn(Cc2ccccc2)c2ccccc12)c1cn(Cc2ccccc2)c2ccccc12
Reaction #7044
product
Ausbeute 78.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C1N(N2CCOCC2)c2ccccc2C1(Cc1ccncc1)Cc1ccncc1
Reaction #50510
desired product
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
CNc1ncn(-c2ccccc2C)c(=O)n1
Reaction #56336
1-(2'-methylphenyl)-4-methylamino-1,2-dihydro-1,3,5-triazin-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CCOC(=O)c1c(N=C=S)sc(C)c1C
Reaction #72658
title compound
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCCCCC1CCC(C=O)CC1
Reaction #76382
4-pentyl-cyclohexanecarboxaldehyde
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
O=C(NCCc1cccc2ccccc12)C1CCC1
Reaction #80567
N-[2-(1-naphthyl)ethyl]cyclobutanecarboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CCN1CCCC1CNC(=O)c1cc(S(=O)(=O)NC)cc2c1OCCO2
Reaction #214593
N-(1-ethyl-2-pyrrolidylmethyl)-7-methylsulfamoyl-1,4-benzodioxane-5-carboxamide
Ausbeute 66.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
Cc1cc2cc(O)ccc2[nH]1
Reaction #216562
product
Ausbeute 67.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
O=C1N(N2CCOCC2)c2ccccc2C1(Cc1ccncc1)Cc1ccncc1
Reaction #322427
desired product
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
CCCCCCCCCCCCCCCCN(C(=O)OCc1ccccc1)c1ccc(C(=O)Cl)cc1
Reaction #350101
N-carbobenzyloxy-4-(hexadecylamino)benzoyl chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_05
CC(C)(C)[Si](C)(C)Oc1cc([N+](=O)[O-])ccc1NC(=S)Nc1ccccc1
Reaction #410206
titled compound
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
COc1ccc(-c2cc(C#N)nnc2-c2ccc(OC)cc2)cc1
Reaction #519842
prisms
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_12
O=C1N(N2CCOCC2)c2ccccc2C1(Cc1ccncc1)Cc1ccncc1
Reaction #527623
desired product
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_05
CCOC(=O)c1c(N=C=S)sc(C)c1C
Reaction #558693
title compound
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
COc1ccc2cccc(CCNC(=O)CCCCl)c2c1
Reaction #570578
N-[2-(7-Methoxynaphth-1-Yl)Ethyl]-4-Chlorobutyramide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_07
COc1ccc2cccc(CCNC(=O)Cc3c[nH]cn3)c2c1
Reaction #570581
N-[2-(7-Methoxynaphth-1-Yl)Ethyl]-4-Imidazolylacetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_07
Cc1cc2ccccn2c1
Reaction #589653
2-methylindolizine
Ausbeute 79.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
CC(C)(C)[Si](C)(C)Oc1cc([N+](=O)[O-])ccc1NC(=S)Nc1ccccc1
Reaction #655148
titled compound
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_01
CC(=O)OC[C@H]1O[C@@H](n2cnc3c2N=CNC3COS(C)(=O)=O)[C@H](OC(C)=O)[C@@H]1OC(C)=O
Reaction #684658
II
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_03
CS(=O)c1ccccc1
Reaction #694526
title compound
Ausbeute 99.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_03
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