MeOH H2O

COC(=O)[C@H](CCCCNC(=O)OCc1ccccc1)NC(=O)OC(C)(C)C.N#N
Reaction #1416
N2 [(1,1-Dimethylethoxy)carbonyl]-N6 -[(phenylmethoxy)carbonyl]-L-lysine, methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)OCC(=O)O
Reaction #4467
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CC(=O)O.CC(=O)O.CC(=O)O.N=C(N)N(CCCCCCCCNCCCCCCCCC1CCCCC1)C1CCCCC1
Reaction #5127
guanidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(=O)O.CC(=O)O.NC1=NCCCN1CCCCCCCCCCCCN1CCCN=C1N
Reaction #5129
guanidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(C)C[C@H](O)[C@H](O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C
Reaction #6073
yellow glass
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C(O)CCCCCO/N=C1/c2ccccc2OC(c2ccccc2)C1n1ccnc1
Reaction #6078
solid
Rendement 67.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Reaction #7578
hydrochloride salt
Rendement 44.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1ccc(C(=O)O)cc1C#N
Reaction #7853
3-cyano-4-methoxy-benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1cccc(-c2nn3c(c2-c2ccnc4ccc(C=CC(=O)O)cc24)CCC3)n1
Reaction #8380
desired product
Rendement 181.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cl.Oc1ccc2c(c1)C1CNCC2C1
Reaction #10200
10-Azatricyclo[6.3.1.02,7]dodeca-2(7),3,5-trien-4-ol hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
N=C(N)Nc1nc2c(s1)CCCC2C(=O)O
Reaction #40320
title compound
Rendement 56.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)n1ncc(C(=O)O)c1C(F)(F)F
Reaction #41142
1-tert-butyl-5-trifluoromethyl-1H-pyrazole-4-carboxylic acid
Rendement 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCCCC.CCO
Reaction #41841
ethanol heptane
Rendement 78.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCNC(=O)O[C@]1(C(=O)CO)[C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@@]21C
Reaction #42656
title compound
Rendement 60.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC[C@@H]1c2cn[nH]c2/C(=N\O)[C@H](CC)N1S(=O)(=O)c1ccc(Cl)cc1
Reaction #44006
product 63
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C/C(=C\C(=O)OCCCCCCCCC(=O)[O-])C[C@@H]1OC[C@H](C[C@@H]2O[C@H]2[C@@H](C)[C@H](C)O)[C@@H](O)[C@H]1O.C/C(=C\C(=O)OCCCCCCCCC(=O)[O-])C[C@@H]1OC[C@H](C[C@@H]2O[C@H]2[C@@H](C)[C@H](C)O)[C@@H](O)[C@H]1O.[Ca+2]
Reaction #44956
product
Rendement 87.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(O)c1ccc2c(c1)S(=O)(=O)NCN2C1CC1
Reaction #46128
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCN(CC)CC[C@H](N)C(=O)O
Reaction #46645
(S)-2-amino-4-(diethylamino)butanoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(O)CSc1nnc(N)s1
Reaction #47798
title compound
Rendement 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COCCCc1nc(C(F)F)ccc1C(=O)O
Reaction #48276
6-Difluoromethyl-2-(3-methoxy-propyl)-nicotinic acid
Rendement 80.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Page 1Suivant