water dioxane

COc1ccccc1NC(=O)c1cccc(CO)c1
Reaction #2545
title compound
Ausbeute 66.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccccc1NC(=O)c1ccc(CO)cc1
Reaction #2546
title compound
Ausbeute 88.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)OC(=O)N[C@@H](CC(=O)O)C(=O)O
Reaction #4528
expected acid
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CCn1cnc2c(Nc3cccc(F)c3)nc(Cl)nc21
Reaction #10007
2-chloro-9-ethyl-6-(3-fluoro-phenyl-amino)-9H-purine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(C)OC(=O)N(Cc1ccccn1)Cc1ccc(C(=O)N[C@@H](CCCNC2CCCc3cccnc32)C(=O)O)cn1
Reaction #11944
title compound
Ausbeute 20.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=Cc1cc2c(nn1)OCCS2
Reaction #43431
solid
Ausbeute 36.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=Cc1cc2c(nn1)SCCO2
Reaction #43433
solid
Ausbeute 31.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(=O)OCc1cc(=O)c(SC(C)(C)C)c[nH]1
Reaction #43438
solid
Ausbeute 100.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=Cc1cc2c(nn1)OCCO2
Reaction #43450
solid
Ausbeute 64.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1c(-c2ccccc2Cl)c(=O)n(C[C@H](N)c2ccccc2)c(=O)n1Cc1c(F)cccc1C(F)(F)F
Reaction #56775
2b
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C(O)CCNC(=O)c1cc(Br)c(Br)[nH]1
Reaction #58058
3-[(4,5-dibromo-1H-pyrrole-2-carbonyl)-amino]-propionic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COc1ccc2c(c1OC(C)C)CCCC2=O
Reaction #62227
35
Ausbeute 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Nc1cccc(-c2nn3c(c2-c2ccncc2)SCC3)c1
Reaction #66351
3-(7-pyridin-4-yl-2,3-dihydro-pyrazolo[5,1-b]thiazol-6-yl)-phenylamine
Ausbeute 73.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Nc1cccc(-c2nn3ccsc3c2-c2ccncc2)c1
Reaction #66371
3-(7-pyridin-4-yl-pyrazolo[5,1-b]thiazol-6-yl)-phenylamine
Ausbeute 68.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(=O)c1csc2c(-c3ccncc3)c(-c3cccc(N)c3)nn12
Reaction #66373
6-(3-amino-phenyl)-7-pyridin-4-yl-pyrazolo[5,1-b]thiazole-3-carboxylic acid ethyl ester
Ausbeute 44.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(N[C@@H](Cc1ccc(O)cc1)C(=O)O)OCC1c2ccccc2-c2ccccc21
Reaction #67545
solid 83
Ausbeute 114.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cn1cc(NC(=O)OC(C)(C)C)cc1-c1nc2ccc(C(=O)O)nc2[nH]1
Reaction #67938
9
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1cc([N+](=O)[O-])cnc1-c1ccccc1
Reaction #70256
3-methyl-5-nitro-2-phenylpyridine
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=[N+]([O-])c1cnc(O)c(-c2ccccc2)c1
Reaction #70258
expected product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=[N+]([O-])c1cnc(Cl)c(-c2ccccc2)c1
Reaction #70263
2-chloro-5-nitro-3-phenylpyridine
Ausbeute 55.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
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