acetonitrile

Cc1c(N2CC[C@@H]([C@H](C)N)C2)c(F)cn2c(=O)c(C(=O)O)cc(C3CC3)c12.Cl
Reaction #1972
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1c(N2CC[C@H]([C@@H](C)N)C2)c(F)cn2c(=O)c(C(=O)O)cc(C3CC3)c12.Cl
Reaction #1973
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1cc(F)cn2c(=O)c(C(=O)O)c(N3CCC(C(C)N)C3)c(C3CC3)c12.Cl
Reaction #1974
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1c(N2CCC(N3CCCCC3)CC2)c(F)cn2c(=O)c(C(=O)O)cc(C3CC3)c12
Reaction #1975
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1c(N2CCN(c3ccccn3)CC2)c(F)cn2c(=O)c(C(=O)O)cc(C3CC3)c12
Reaction #1976
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1c(N2CCC(C(C)(C)N)C2)c(F)cn2c(=O)c(C(=O)O)cc(C3CC3)c12.Cl
Reaction #1977
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCC(N)C1CCN(c2c(F)cn3c(=O)c(C(=O)O)cc(C4CC4)c3c2C)C1.Cl
Reaction #1978
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C#CCOc1cc(-n2nc3n(c2=O)CC(O)CC3)c(Cl)cc1Cl
Reaction #2059
title product
Ausbeute 36.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C1NN=C(c2ccc(Cl)cc2)CS1
Reaction #2183
5-(4-chlorophenyl)-3H,6H-1,3,4-thiadiazin-2-one
Ausbeute 48.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C1NN=C(c2ccc(Cl)cc2)CS1
Reaction #2224
5-(4-chlorophenyl)-3H,6H-1,3,4-thiadiazin-2-one
Ausbeute 48.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Br.COC(=O)Cn1ccc(=Nc2noc3ccccc23)cc1
Reaction #2245
title compound
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C1NN=C(c2ccc(Cl)cc2)CS1
Reaction #2282
5-(4-chlorophenyl)-3H,6H-1,3,4-thiadiazin-2-one
Ausbeute 48.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)COc1ccc(C(=O)CN2CCN(c3ccncc3)CC2)cc1
Reaction #2296
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)Cc1ccc(C(=O)CN2CCN(c3ccncc3)CC2)cc1
Reaction #2300
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)COc1ccc(C(=O)C(C)N2CCN(c3ccncc3)CC2)cc1
Reaction #2301
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)C(C)(C)Oc1ccc(C(=O)CN2CCN(c3ccncc3)CC2)cc1
Reaction #2313
methyl 2-[4-[2-[4-(4-pyridyl)piperazin-1-yl]acetyl]phenoxy]isobutyrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)COc1ccc(C(=O)CN2CCN(c3ccncc3)CC2)cc1
Reaction #2314
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)OC(=O)COc1ccc(C(=O)CN2CCN(c3ccncc3)CC2)cc1
Reaction #2315
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)COc1ccc(C(=O)C(C)(C)N2CCN(c3ccncc3)CC2)cc1
Reaction #2328
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)COc1ccc(C(=O)C(C)CN2CCN(c3ccncc3)CC2)cc1
Reaction #2330
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
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