子结构搜索

273738

CCCOc1ccc(Br)cc1-c1nc2c(CCC)nn(C)c2c(=O)[nH]1
Reaction #50204
title compound
收率 83.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCOc1ccc(/C=C/C(=O)OC(C)(C)C)cc1-c1nc2c(CCC)nn(C)c2c(=O)[nH]1
Reaction #50205
title compound
收率 378.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nn(C)c2c(=O)[nH]c(-c3cc(Br)ccc3OCC)nc12
Reaction #50207
5-(5-Bromo-2-ethoxyphenyl)-1-methyl-3-n-propyl-1,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one
DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nn(C)c2c(=O)[nH]c(-c3cc(/C=C/C(=O)N(C)C)ccc3OCC)nc12
Reaction #50209
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #50210
crystals
收率 33.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nn(C)c2c(=O)[nH]c(-c3cc(-n4ccnc4)ccc3OCC)nc12
Reaction #50213
title compound
收率 38.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nn(C)c2c(=O)[nH]c(-c3cc(-c4nccn4C)ccc3OCC)nc12
Reaction #50214
title compound
收率 53.1%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #50215
solid
收率 33.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nn(C)c2c(=O)[nH]c(-c3cc(C=CC#N)ccc3OCC)nc12
Reaction #195330
DOI: 10.1039/C8SC04228D
CCCc1nn(C)c2c(=O)[nH]c(-c3cc(-n4ccnc4)ccc3OCC)nc12
Reaction #244725
DOI: 10.1039/C8SC04228D
CCCc1nn(C)c2c(=O)[nH]c(-c3cc(C=CC(=O)N(C)C)ccc3OCC)nc12
Reaction #389711
DOI: 10.1039/C8SC04228D
CCCOc1ccc(Br)cc1-c1nc2c(CCC)nn(C)c2c(=O)[nH]1
Reaction #414224
title compound
收率 83.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCOc1ccc(/C=C/C(=O)OC(C)(C)C)cc1-c1nc2c(CCC)nn(C)c2c(=O)[nH]1
Reaction #414225
title compound
收率 58.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nn(C)c2c(=O)[nH]c(-c3cc(Br)ccc3OCC)nc12
Reaction #414227
5-(5-Bromo-2-ethoxyphenyl)-1-methyl-3-n-propyl-1,6-dihydro-7H-pyrazolo[4,3-d]-pyrimidin-7-one
DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nn(C)c2c1N=C(c1cc(/C=C/C(=O)N(C)C)ccc1OCC)NC2
Reaction #414229
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #414230
crystals
收率 33.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nn(C)c2c(=O)[nH]c(-c3cc(-n4ccnc4)ccc3OCC)nc12
Reaction #414233
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #414234
solid
收率 33.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCOc1ccc(C=CC(=O)OC(C)(C)C)cc1-c1nc2c(CCC)nn(C)c2c(=O)[nH]1
Reaction #750635
DOI: 10.1039/C8SC04228D
CCCOc1ccc(Br)cc1-c1nc2c(CCC)nn(C)c2c(=O)[nH]1
Reaction #763392
DOI: 10.1039/C8SC04228D
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