部分構造検索

CC1=C(OC(=N1)N)C

Cc1nc(Nc2cc(Cl)ccn2)oc1C
Reaction #408
収率 15.2%
Cc1nc(Nc2cc(Cl)ccn2)oc1C
Reaction #409
収率 15.2%
Cc1nc(N)oc1-c1cccc2ccccc12
Reaction #61837
title compound ( 3 )
収率 22.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1nc(N)oc1-c1cccc2ccccc12
Reaction #61839
title compound ( 7 )
DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(CCl)c(-c2cccc3ccccc23)o1
Reaction #61853
4-chloromethyl-5-naphthalen-1-yl-oxazol-2-ylamine
収率 45.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1oc(N)nc1-c1cccc2ccccc12
Reaction #61854
5-methyl-4-naphthalen-1-yl-oxazol-2-ylamine
収率 14.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1nc(N)oc1-c1ccc(F)c2ccccc12
Reaction #61857
title compound
収率 6.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc2c(o1)CCc1ncccc1-2
Reaction #62936
4,5-Dihydrooxazolo[4,5-f]quinolin-2-amine
DOI: 10.6084/m9.figshare.5104873.v1
CCCN1CCC=C2c3oc(N)nc3CCC21
Reaction #62937
(±) 4,5,5a,6,7,8-hexahydro-6-propyloxazolo [5,4-f]quinolin-2-amine
DOI: 10.6084/m9.figshare.5104873.v1
CCCN1CCC[C@H]2c3nc(N)oc3CC[C@@H]21
Reaction #62938
(±) trans-4,5,5a,6,7,8,9,9a-octahydro-6-propyloxazolo[4,5-f]quinolin-2-amine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1nc(N2CC[C@H](NC(=O)OCc3ccccc3)[C@H](OC)C2)oc1C
Reaction #71894
title compound
収率 78.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)c1nc(N2CC[C@H](N)[C@H](OC)C2)oc1C
Reaction #71895
title compound
収率 113.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1oc(N2CC[C@H](NC(=O)OCc3ccccc3)[C@H](OC)C2)nc1C
Reaction #71897
title compound
収率 31.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1oc(N2CC[C@H](N)[C@H](OC)C2)nc1C
Reaction #71898
title compound
収率 100.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1nc(N2CC[C@H](NC(=O)OCc3ccccc3)[C@H](OC)C2)oc1CC
Reaction #71916
title compound
収率 108.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)c1nc(N2CC[C@H](N)[C@H](OC)C2)oc1CC
Reaction #71917
title compound
収率 107.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)c1nc(N2CC[C@H](NC(=O)c3nc(Cl)c(CC)[nH]3)[C@H](OC)C2)oc1CC
Reaction #71918
title compound
収率 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1nc(N2CC[C@H](NC(=O)OCc3ccccc3)[C@H](OC)C2)oc1C(C)C
Reaction #71921
title compound
収率 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)c1nc(N2CC[C@H](N)[C@H](OC)C2)oc1C(C)C
Reaction #71922
title compound
収率 96.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)c1nc(N2CC[C@H](NC(=O)c3nc(Cl)c(CC)[nH]3)[C@H](OC)C2)oc1C(C)C
Reaction #71923
title compound
収率 80.6%DOI: 10.6084/m9.figshare.5104873.v1
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