phosphorus oxybromide

BrCc1cccc(-c2ncccn2)c1
Reaction #69863
title compound
수율 80.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1cnc(-c2cccc(CBr)c2)o1
Reaction #69881
title compound
수율 84.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=[N+]([O-])c1cnc(Br)c(-c2ccccc2)c1
Reaction #70259
expected product
수율 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=[N+]([O-])c1cnc(Br)c(Br)c1
Reaction #70272
expected product
수율 73.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Clc1nn2c(Br)nnc2cc1N1CCOCC1
Reaction #75511
3-bromo-6-chloro-7-(morpholin-4-yl)-1,2,4-triazolo[4,3-b]pyridazine
수율 43.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
Cc1ccnc(Br)c1[N+](=O)[O-]
Reaction #88236
title compound
수율 71.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C1c2ccccc2CCc2c1nc1c(cnn1Cc1ccccc1)c2Br
Reaction #94060
1-benzyl-4-bromo-5,6-dihydrobenzo[5,6]cyclohepta[1,2-b]pyrazolo[4,3-e]pyridin-11(1H)one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
CCc1cc(C(F)(C(F)(F)F)C(F)(F)C(F)(F)F)cc(C)c1NC(=O)c1ccc2nc(C#N)cc(Br)c2c1
Reaction #157996
4-bromo-2-cyano-N-[2-ethyl-6-methyl-4-(1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl)phenyl]quinoline-6-carboxamide
수율 43.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCn1c(=O)c(Br)nc2ccccc21
Reaction #163545
3-bromo-1-ethyl-quinoxalin-2(1H)-one
수율 53.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(O)c1cc(Br)nc2ccccc12
Reaction #181699
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)c1ccc(C(F)(F)F)nc1Br
Reaction #184249
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cc(Br)cc(=O)[nH]1
Reaction #186631
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cc(Cc2cc(C)cc(C(C)(C)C)c2O)c(O)c(C(C)(C)C)c1
Reaction #192763
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
FC(F)(F)c1cc(Br)nc(-c2ccc(Cl)cc2)c1
Reaction #206034
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
FC(F)(F)c1cc(Br)c2ccccc2n1
Reaction #222281
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)C(C)Oc1ccc(N(C)c2cc3ccc(Cl)cc3c(Br)n2)cc1
Reaction #231050
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)C(Br)c1cnc(Cl)nc1Cl
Reaction #236486
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1cc(C)cc(-c2ccc3[c]([Sn]([CH3])([CH3])[CH3])c4ccccc4nc3c2)c1
Reaction #237641
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)Cn1ccnc(Br)c1=O
Reaction #249435
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CSc1ncc2c(Br)cc(=O)n(C3CCCC3)c2n1
Reaction #249668
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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