6-bromo-1H-indazole

Clc1ccccc1Nc1ccc2cn[nH]c2c1
Reaction #337
Yield 0.0%750 AstraZeneca ELN dataset
c1cc2cn[nH]c2cc1N1CCCC1
Reaction #648
Yield 93.7%750 AstraZeneca ELN dataset
CC(C)(C)OC(=O)N1CC=C(c2ccc3cn[nH]c3c2)CC1
Reaction #155929
4-(1H-indazol-6-yl)-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)(C)OC(=O)Cc1ccc2cn[nH]c2c1
Reaction #169405
title compound
Yield 65.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Brc1ccc2cn(Cc3ccccc3)nc2c1
Reaction #241216
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
C[Si](C)(C)CCOCn1ncc2ccc(Br)cc21
Reaction #332985
6-bromo-1-(2-trimethylsilanyl-ethoxymethyl)-1H-indazole
Yield 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
C=Cc1ccc2cn[nH]c2c1
Reaction #333217
6-vinyl-1H-indazole
Yield 79.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
Cn1ncc2ccc(Br)cc21
Reaction #560965
6-bromo-1-methylindazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
Cn1ncc2ccc(Br)cc21
Reaction #588453
1-methyl-6-bromoindazole
Yield 51.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
CC(=O)c1ccc2cn[nH]c2c1
Reaction #601541
title compound 24-a
Yield 9.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_08
CC(=O)c1ccc2cn[nH]c2c1
Reaction #965698
title compound 24-a
Yield 9.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_03
c1ccc2[nH]ncc2c1
Reaction #1023745
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
Cn1ncc2ccc(Br)cc21
Reaction #1031510
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
OC(COc1cccc(-c2ccc3cn[nH]c3c2)c1)CN1CCc2ccccc2C1
Reaction #1138631
title compound
Yield 16.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_07
COc1ccc(S(=O)(=O)n2ncc3ccc(Br)cc32)cc1
Reaction #1139712
title compound
Yield 87.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_07
COc1ncccc1Nc1ncnc(-n2ncc3ccc(Br)cc32)n1
Reaction #1485681
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_12
OC(COc1cccc(-c2ccc3cn[nH]c3c2)c1)CN1CCc2ccccc2C1
Reaction #1487000
title compound
Yield 16.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_12
Brc1ccc2cn(Cc3ccccc3)nc2c1
Reaction #1497517
N2-benzyl-6-bromo-2H-indazole
Yield 35.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_12
Cn1ncc2ccc(Br)cc21
Reaction #1564580
6-bromo-1-methylindazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_08
O=Cc1ccc2cn[nH]c2c1
Reaction #1702378
title compound
Yield 58.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_07
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