TBTU

C[C@@H](C(=O)N1CCOCC1)N1CC[C@H](NC(=O)OCc2ccccc2)C1=O
Reaction #7386
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)C(C)NC(=O)c1ccc(Cl)s1
Reaction #43375
methyl 2-[(5-chloro-thiophene-2-carbonyl)-amino]-propionate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(NC(=O)c1ccc(Cl)s1)C(=O)Nc1ccc(C(=O)N2CCCC2)c(Cl)c1
Reaction #43377
5-chloro-thiophene-2-carboxylic acid-N-{1-[3-chloro-4-(pyrrolidin-1-yl-carbonyl)-phenylcarbamoyl]-ethyl}-amide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(c1ccc([N+](=O)[O-])cc1Br)N1CCCC1
Reaction #43380
3-bromo-4-(pyrrolidin-1-yl-carbonyl)-1-nitro-benzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C[C@@H](NC(=O)c1ccc(Cl)s1)C(=O)OC(C)(C)C
Reaction #43381
tert.-butyl(R)-2-[(5-chloro-thiophene-2-carbonyl)-amino]-propionate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1cc(NC(=O)C(C)(C)NC(=O)c2ccc(Cl)s2)ccc1C(=O)N1CCCCC1CCCO
Reaction #43386
5-chloro-thiophene-2-carboxylic acid-N-{1-methyl-1-[3-methyl-4-(2-{3-hydroxy-prop-1-yl}-piperidin-1-yl-carbonyl)-phenylcarbamoyl]-ethyl}-amide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cl.O=C(NC1CN2CCC1CC2)c1cc2cc([N+](=O)[O-])ccc2s1
Reaction #43730
hydrochloride
المردود 48.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C[C@@]1(Cc2ccc(C#N)cc2)C(=O)N(c2cc(Cl)cc(Cl)c2)c2ncc(S(=O)(=O)N3CCC[C@H]3C(=O)NC[C@H]3CCC(=O)O3)n21
Reaction #52118
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COCCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1cnc2n1[C@](C)(Cc1ccc(-c3cncnc3)cc1)C(=O)N2c1cc(Cl)cc(Cl)c1
Reaction #52119
title compound
المردود 44.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
C[C@@H](NC(=O)[C@@H]1CCCN1S(=O)(=O)c1cnc2n1[C@](C)(Cc1ccc(-c3cncnc3)cc1)C(=O)N2c1cc(Cl)cc(Cl)c1)C(=O)O
Reaction #52120
title compound
المردود 44.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
C[C@@]1(Cc2ccc(-c3cncnc3)cc2)C(=O)N(c2cc(Cl)cc(Cl)c2)c2ncc(S(=O)(=O)N3CCC[C@H]3C(=O)NCCC(N)=O)n21
Reaction #52121
title compound
المردود 10.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
Cn1c(CCc2ccc(C#N)cc2)nc2cc(C(=O)NN3CCN(CC=Cc4ccccc4)CC3)ccc21
Reaction #52189
2-[2-(4-Cyanophenyl)-ethyl]-1-methyl-benzimidazole-5-yl-carboxylic acid-[4-(3-phenyl-allyl)-piperazinyl]-amide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CC(=O)N1C(=O)C(=C(O)c2ccccc2)c2ccccc21
Reaction #53005
1-acetyl-3-(1-hydroxy-1-phenyl-methylidene)-2-indolinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CN(C)C(=O)c1ccc(N/C(=C2\C(=O)Nc3ccccc32)c2ccccc2)cc1
Reaction #53026
(Z)-3-[1-(4-dimethylaminocarbonyl-phenylamino)-1-phenyl-me-thylidene]-2-indolinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CNC(=O)c1ccc(N/C(=C2\C(=O)Nc3ccccc32)c2ccccc2)cc1
Reaction #53027
(Z)-3-[1-(4-methylaminocarbonyl-phenylamino)-1-phenyl-me-thylidene]-2-indolinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CNC(=O)c1cccc(N/C(=C2\C(=O)Nc3ccccc32)c2ccccc2)c1
Reaction #53029
(Z)-3-[1-(3-methylaminocarbonyl-phenylamino)-1-phenyl-methylidene]-2-indolinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CN(C)C(=O)c1cccc(N/C(=C2\C(=O)Nc3ccccc32)c2ccccc2)c1
Reaction #53030
(Z)-3-[1-(3-dimethylaminocarbonyl-phenylamino)-1-phenyl-methylidene]-2-indolinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCOC(=O)CNC(=O)c1cccc(N/C(=C2\C(=O)Nc3ccccc32)c2ccccc2)c1
Reaction #53031
(Z)-3-[1-(3-ethoxycarbonylmethylaminocarbonyl-phenylamino)-1-phenyl-methylidene]-2-indolinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCOC(=O)CN(C)C(=O)c1cccc(N/C(=C2\C(=O)Nc3ccccc32)c2ccccc2)c1
Reaction #53033
(Z)-3-{1-[3-(N-ethoxycarbonylmethyl-N-methyl-aminocarbonyl)-phenylamino]-1-phenyl-methylidene}-2-indolinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CC(C)(C)OC(=O)NCC(=O)Nc1ccc(N/C(=C2\C(=O)Nc3ccccc32)c2ccccc2)cc1
Reaction #53041
(Z)-3-[1-(4-tert.butoxycarbonylaminomethylcarbonylamino-phenylamino)-1-phenyl-methylidene]-2-indolinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
الصفحة 1التالي