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Cc1cc(Cl)cc2c(=O)oc(-c3cc(Br)nn3-c3ncccc3Cl)nc12
Reaction #90223
title product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(Cl)nn1-c1ncccc1Cl
Reaction #90228
3-chloro-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(Br)nn1-c1ncccc1Cl
Reaction #90229
3-bromo-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Cl)cc2c(=O)oc(-c3cc(Br)nn3-c3ncccc3Cl)nc12
Reaction #90237
title product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(Br)nn1-c1ncccc1Cl
Reaction #201689
DOI: 10.1039/C8SC04228D
CNC(=O)c1cc(C#N)cc(C)c1NC(=O)c1cc(Br)nn1-c1ncccc1Cl
Reaction #222196
DOI: 10.1039/C8SC04228D
O=C(Nc1c(F)cc(F)cc1Br)c1cc(Br)nn1-c1ncccc1Cl
Reaction #288542
DOI: 10.1039/C8SC04228D
O=C(O)c1cc(Br)nn1-c1ncccc1Cl
Reaction #301274
DOI: 10.1039/C8SC04228D
Cc1cc2cn[nH]c2c2c(=O)oc(-c3cc(Br)nn3-c3ncccc3Cl)nc12
Reaction #332801
7-[5-bromo-2-(3-chloro-pyridin-2-yl)-2H-pyrazol-3-yl]-5-methyl-1H-8-oxa-1,2,6-triaza-cyclopenta[a]naphthalen-9-one
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Cl)cc2c(=O)oc(-c3cc(Br)nn3-c3ncccc3Cl)nc12
Reaction #339087
2-[3-bromo-1-(3-chloro-2-pyridinyl)-1H-pyrazol-5-yl]-6-chloro-8-methyl-4H-3,1-benzoxazine-4-one
Ausbeute 14.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(Br)nn1-c1ncccc1Cl
Reaction #339097
3-bromo-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(I)cc2c(=O)oc(-c3cc(Br)nn3-c3ncccc3Cl)nc12
Reaction #341611
title product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)c1cc(Br)nn1-c1ncccc1Cl
Reaction #399278
DOI: 10.1039/C8SC04228D
O=C(Cl)c1cc(Br)nn1-c1ncc(Cl)cc1Cl
Reaction #408192
DOI: 10.1039/C8SC04228D
CNC(=O)c1cc(C#N)cc(C)c1NC(=O)c1cc(Br)nn1-c1ncccc1Cl
Reaction #492012
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(I)cc2c(=O)oc(-c3cc(Br)nn3-c3ncccc3Cl)nc12
Reaction #531826
title product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(Br)nn1-c1ncc(Cl)cc1Cl
Reaction #540264
product
Ausbeute 81.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(Br)nn1-c1ncc(Cl)cc1Cl
Reaction #540265
product
Ausbeute 52.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)c1cc(Br)nn1-c1ncc(Cl)cc1Cl
Reaction #540266
product
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
O=c1oc(-c2cc(Br)nn2-c2ncc(Cl)cc2Cl)nc2c(Cl)cc(Cl)cc12
Reaction #540267
product
Ausbeute 45.0%DOI: 10.6084/m9.figshare.5104873.v1
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