HCl

Cl.NCCCC[C@@H](N)C(=O)O
Reaction #891
D-lysine monohydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1cc(C=O)c(C)c2c1SCCC2(C)C
Reaction #894
desired compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=O)Nc1cccc(C)c1C(=O)O
Reaction #900
2-Methyl-6-acetamidobenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1c([N+](=O)[O-])ccc(N)c1C(=O)O
Reaction #902
2-Methyl-3-nitro-6-aminobenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1c(I)ccc2c1C(=O)NS2(=O)=O
Reaction #906
iodine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C#CCC1C(=O)N(C)OC1c1ccccc1
Reaction #907
2-methyl-5-phenyl-4-propargylisoxazolin-3-one
Rendement 34.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1c(S(=O)(=O)NC(C)(C)C)ccn1C
Reaction #909
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1c(S(=O)(=O)NC(C)(C)C)ccn1C
Reaction #910
title compound
Rendement 55.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CSc1c(S(=O)(=O)NC(C)(C)C)ccn1C
Reaction #912
title compound
Rendement 58.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cn1ccc(S(=O)(=O)NC(C)(C)C)c1Br
Reaction #914
title compound
Rendement 58.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cn1ccc(S(=O)(=O)NC(C)(C)C)c1C=O
Reaction #916
title compound
Rendement 39.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN(C)C(=O)c1c(S(=O)(=O)NC(C)(C)C)ccn1C
Reaction #921
title compound
Rendement 50.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1ccn(C)c1S(=O)(=O)NC(=O)NC1=NC(OC)=CN(C)N1
Reaction #925
oil
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N#Cc1c(N)cccc1Sc1ccccc1
Reaction #930
2-Amino-6-(phenylthio)benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1cc(C)cc(Sc2cccc(N)c2C#N)c1
Reaction #932
2-amino-6-[(3,5-dimethylphenyl)thio]benzonitrile
Rendement 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC1(COS(=O)(=O)c2ccc(C)cc2)COC(=O)N1
Reaction #949
beige solid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
[N-]=[N+]=NCc1ccc(C(=N)NC(=O)OCc2ccccc2)cc1
Reaction #952
4-(benzyloxycarbonylamidino) benzyl azide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N=C(NC(=O)OCc1ccccc1)N1CCC(CCN)CC1
Reaction #957
4-Aminoethyl-1-benzyloxycarbonylamidino piperidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)[Si](OCc1ccc(CCCC=O)cc1)(c1ccccc1)c1ccccc1
Reaction #987
aldehyde
Rendement 42.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)c1c[nH]c2c1C(=O)CCCC2
Reaction #1002
4-oxo-1,4,5,6,7,8-hexahydro-cyclohepta[b]pyrrole-3-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
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