ethyl ethanimidate;hydrochloride

CC(=N)NNC(=O)c1cn(C)c(=O)c(F)c1Nc1ccc(Br)cc1F
Reaction #44203
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(=N)N(N)C(=O)c1ccc(C)cc1
Reaction #58075
solid
Ausbeute 15.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(=N)N(N)C(=O)c1ccc(F)cc1
Reaction #58077
4-fluoro-benzoic acid-(1-imino-ethyl)-hydrazide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COC(=O)c1cccc(C(=O)NNC(C)=N)c1
Reaction #58083
methyl 3-[N′-(1-imino-ethyl)-hydrazinocarbonyl]-benzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(=N)NNC(=O)c1ccc(C(F)(F)F)cc1
Reaction #58087
4-trifluoromethyl-benzoic acid N′-(1-imino-ethyl)-hydrazide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COc1ccc(C(=O)NNC(C)=N)cc1
Reaction #58090
4-methoxy-benzoic acid N′-(1-imino-ethyl)-hydrazide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Cc1nc2cc(C(C(C)C)n3ccnc3)ccc2[nH]1.Cl.Cl
Reaction #65494
5-[1-(1H-imidazol-1yl)-2-methylpropyl]-2-methyl-1H-benzimidazole dihydrochloride
Ausbeute 44.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CCOC(=O)C(Cc1ccc2ccc(C(=N)N)cc2c1)c1ccc(O[C@H]2CCN(C(C)=N)C2)cc1.Cl.Cl
Reaction #82280
title compound
Ausbeute 193.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CC(=N)N1CC[C@H](Oc2ccc(C(Cc3cc4cc(C(=N)N)ccc4o3)C(=O)O)cc2)C1.Cl.Cl
Reaction #82284
title compound
Ausbeute 130.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CCOC(=O)C(Cc1cc2cc(C(=N)N)ccc2s1)(C(=O)OCC)c1ccc(OC[C@H]2CCCN2C(C)=N)cc1.Cl.Cl
Reaction #82285
ethyl 2-[4-[((2R)-1-acetimidoyl-2-pyrrolidinyl)methoxy]phenyl]-2-ethoxycarbonyl-3-(5-amidinobenzo[b]thien-2-yl)propionate dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
COc1cc(NC(=O)c2ccccc2Cl)ccc1C(=O)N1CCCC(OCCNC(C)=N)c2cc(Cl)ccc21.Cl
Reaction #83033
5-[2-(1-iminoethyl)aminoethoxy]-7-chloro-1-[2-methoxy-4-(2-chlorobenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzo-azepine hydrochloride
Ausbeute 69.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
Cc1nc2cc(-c3nc4cc(Cl)ccc4o3)ccc2n1CCC(F)(F)F
Reaction #161501
title compound
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COCCNC(=O)c1nc(N[C@H]2CCCC[C@H]2NC(C)=N)c2cc(C)ccc2n1
Reaction #162708
desired compound
Ausbeute 77.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COc1cc(O)c2c(c1C)C(=O)OCCCCC(=S)N[C@H](c1nc(CNC(C)=N)no1)CSC2
Reaction #321423
(4R)-N-[5-(16-hydroxy-14-methoxy-13-methyl-12-oxo-6-thioxo-1,3,4,5,6,7,8,9,10,12-decahydro-11,2,5-benzoxathiaazacyclotetradecin-4-yl)-1,2,4-oxadiazol-3-ylmethyl]-acetimidamide
Ausbeute 24.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
CC(=N)N1CCC(N(Cc2ncccc2C)Cc2ncccc2C)CC1
Reaction #338365
COMPOUND 338
Ausbeute 34.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
CC(=N)N1CCC(c2ccc(C(=O)N3CCN(S(=O)(=O)c4ccc5cc(Cl)ccc5c4)CC3)cc2)CC1.Cl
Reaction #365790
title compound
Ausbeute 195.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
N=C(N)Nc1nc(C(=O)O)cs1
Reaction #367919
2-guanidino-4-thiazole carboxylic acid
Ausbeute 128.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_05
CC(=N)NCCCC[C@H](N)C(=O)O.Cl
Reaction #431007
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
CC(=N)N1C[C@@H](SC2=C(C(=O)O)N3C(=O)[C@H]([C@@H](C)O)[C@H]3[C@H]2C)C[C@H]1COCCO
Reaction #433562
(4R,5S,6S)-3-[(2S,4S)-1-acetimidoyl-2-(2-hydroxyethyloxymethyl)pyrrolidin-4-ylthio]-6-[(1R)-1-hydroxyethyl]- 4-methyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid
Ausbeute 87.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_10
CC(=N)N1CC[C@H](Oc2ccc(C(Cc3cc4cc(C(=N)N)ccc4o3)C(=O)O)cc2)C1.Cl.Cl
Reaction #449122
title compound
Ausbeute 130.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_02
Seite 1Weiter