tin

COc1ccccc1N(CCN1CCC(C(=O)c2ccc(F)cc2)CC1)C(=O)c1ccc(N)cc1
Reaction #2572
title compound
収率 98.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCn1c(=O)c2[nH]c(N)nc2n(CCCC)c1=O.Cl
Reaction #3726
1,3-Di-n-butyl-8-amino Xanthine Hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1cccc(NN)c1.Cl
Reaction #4479
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
C=Cc1ccc2nc(NC(=O)NCC)sc2c1C=C
Reaction #9220
desired compound
収率 39.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCCCOC(=O)CCC
Reaction #56512
butylbutyrate
収率 45.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CCCC=O
Reaction #56513
n-butyraldehyde
収率 45.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CCn1cc(-c2c(F)cnc3[nH]ccc23)c(-c2ccc(N)cc2)n1
Reaction #57199
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C(O)Cn1cc(-c2ccnc3[nH]ccc23)c(-c2ccc(NC(=O)Nc3ccccc3)cc2)n1
Reaction #57209
title compound
収率 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
NC1=c2ccsc2=NCN1c1ccc(N)cc1
Reaction #60767
4-Amino-3-(4-aminophenyl)thieno[2,3-d]pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
—
Reaction #62163
salt
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(C)(C)N(CC(=O)O)Cc1c(N)ccc(Cl)c1Cl
Reaction #69630
1,1-dimethyl-ethyl-(6-amino-2,3-dichlorobenzyl)glycine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Nc1ccc2c3c(cccc13)CC2
Reaction #74890
5-aminoacenaphthene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
C=CCOC(=O)c1c(Oc2nc(OC)cc(OC)n2)ccc2[nH]c(C)c(N)c12
Reaction #80291
desired product
収率 79.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
C=CC(=O)OCCCCCC(C)C
Reaction #173375
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCc1cc(C(=O)c2c(Cc3ccccc3)oc(C)c2C)cc(CC)c1OC
Reaction #185525
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Nc1ccc(C(F)(F)F)cc1N
Reaction #189088
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc(OC)c(C(=O)O)cc1S
Reaction #192302
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Oc1ccc2cc(Br)ccc2c1
Reaction #192633
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)c1ccc(N)cc1F
Reaction #192797
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)c1ccc(NC(=O)c2cccc(N)c2)cc1
Reaction #194744
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
1 ページ次のページ