部分構造検索

Clc1noc2ccccc12

CC(C)(C)OC(=O)N1CCN(c2noc3ccccc23)CC1
Reaction #61875
desired product
収率 42.0%DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc2onc(OCC(Cc3cn(C(c4ccccc4)(c4ccccc4)c4ccccc4)cn3)NC(c3ccccc3)(c3ccccc3)c3ccccc3)c2c1
Reaction #190014
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCN(c2noc3ccccc23)CC1
Reaction #220116
desired product
収率 42.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc2onc(Cl)c2c1
Reaction #227401
DOI: 10.1039/C8SC04228D
FC(F)(F)c1cc(C(F)(F)F)n(-c2ccc(Nc3noc4ccccc34)cc2)n1
Reaction #285830
DOI: 10.1039/C8SC04228D
OCCCCNc1noc2ccccc12
Reaction #292646
DOI: 10.1039/C8SC04228D
Clc1ccc2c(N3CCNCC3)noc2c1
Reaction #328762
6-chloro-3-piperazinyl-benzisoxazole
収率 71.1%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1cc2c(Cl)noc2c(F)c1F
Reaction #332711
product
収率 115.6%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(c2c(C=O)cc3c(Cl)noc3c2F)C[C@H](C)O1
Reaction #332713
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(c2c(C=O)cc3c(Cl)noc3c2F)C[C@@H](C)O1
Reaction #332714
3-chloro-6-((2R,6R)-2,6-dimethylmorpholino)-7-fluorobenzo[d]isoxazole-5-carbaldehyde
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(c2c(C=O)cc3c(-n4cncn4)noc3c2F)C[C@H](C)O1
Reaction #332718
title product
DOI: 10.6084/m9.figshare.5104873.v1
CSc1noc2c(F)c(N3C[C@@H](C)O[C@@H](C)C3)c(C=O)cc12
Reaction #332719
6-[(2R,6S)-2,6-dimethylmorpholin-4-yl]-7-fluoro-3-(methylsulfanyl)-1,2-benzoxazole-5-carbaldehyde
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C)n(-c2noc3c(F)c(N4C[C@@H](C)O[C@@H](C)C4)c(C=O)cc23)n1
Reaction #332720
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(c2c(C=O)cc3c(-c4cn[nH]c4)noc3c2F)C[C@H](C)O1
Reaction #332721
6-[(2R,6S)-2,6-dimethylmorpholin-4-yl]-7-fluoro-3-(1H-pyrazol-4-yl)-1,2-benzoxazole-5-carbaldehyde
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(c2c(C=O)cc3c(-n4cncn4)noc3c2F)C[C@@H](C)O1
Reaction #332725
desired product
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN2c3c(cc4c(Cl)noc4c3F)CC3(C(=O)NC(=O)NC3=O)[C@H]2[C@H](C)O1
Reaction #332757
product
収率 26.5%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC(Oc2noc3ccc(Cl)cc23)CC1
Reaction #350640
title compound
収率 67.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2noc3ccccc23)CC1
Reaction #358968
desired product
収率 42.0%DOI: 10.6084/m9.figshare.5104873.v1
OCCCCNc1noc2ccccc12
Reaction #362926
4-(1,2-benzisoxazol-3-ylamino)-1-butanol
収率 93.3%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #364548
methylene chloride hexanes
DOI: 10.6084/m9.figshare.5104873.v1
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