An 14 Reaktionen beteiligt

1197897

O=c1[nH]c2c(c(=O)[nH]1)CCCC2
Reaction #72655
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(=O)c1oc2c(c1N)CCCC2
Reaction #302931
desired product
Ausbeute 42.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
N#CC1=C(Nc2ccc(F)cc2)CCCC1
Reaction #453582
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
O=c1[nH]c2c(c(=O)[nH]1)CCCC2
Reaction #558690
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
O=c1[nH]c2c(c(=O)[nH]1)CCCC2
Reaction #798828
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
Cc1ccccc1-n1nc2c(c1N)CCCC2
Reaction #1002748
2-(2-methylphenyl)-4,5,6,7-tetrahydro-2H-indazol-3-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_09
CCOC(=O)c1oc2c(c1N)CCCC2
Reaction #1515417
desired product
Ausbeute 42.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_01
Nc1c2c(nn1-c1ccc(Cl)cc1)CCCC2
Reaction #1526528
3-amino-2-(4-chlorophenyl)-4,5,6,7-tetrahydro-2H-indazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_11
Cn1nc2c(c1N)CCCC2
Reaction #1564935
desired product 17
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_08
Cn1nc2c(c1N)CCCC2
Reaction #1564944
desired product 124
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_08
O=c1[nH]c2c(c(=O)[nH]1)CCCC2
Reaction #2164174
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_04
CCOC(=O)c1oc2c(c1N)CCCC2
Reaction #2178684
desired product
Ausbeute 42.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_05
CCOC(=O)c1oc2c(c1N)CCCC2
Reaction #2180511
desired product
Ausbeute 42.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_05
Nc1c2c(nn1-c1ccc(Cl)cc1)CCCC2
Reaction #2507159
3-amino-2-(4-chlorophenyl)-4,5,6,7-tetrahydro-2H-indazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_08