Recherche de Sous-structure

6453

c1cc2cc3c(cc2[nH]1)OCO3
Reaction #4575
5,6-Methylenedioxyindole
DOI: 10.6084/m9.figshare.5104873.v1
O=C=Nc1ccc2c(c1)OCO2
Reaction #5945
3,4-methylenedioxyphenylisocyanate
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(Nc1ccc2c(c1)OCO2)OCCCN1CCN(c2cccc(Cl)c2)CC1
Reaction #5946
title compound
Rendement 187.1%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCN1C(=O)c2cccc3cc4cccc(NC(=O)Nc5ccc6c(c5)OCO6)c4c(c23)C1=O
Reaction #46408
desired product
Rendement 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCN1C(=O)c2cccc3cc4c(NC(=O)Nc5ccc6c(c5)OCO6)cccc4c(c23)C1=O
Reaction #46410
desired product
Rendement 51.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C=Nc1ccc2c(c1Cl)OCO2
Reaction #47221
4-chloro-5-isocyanatobenzo[d][1,3]dioxole
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2c(cc1N)OCO2
Reaction #61076
title compound
Rendement 94.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC(c2ccccc2F)=Nc2ccc(O)c(O)c21
Reaction #66911
40
Rendement 13.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC(c2cccc3ccccc23)=Nc2cc3c(cc21)OCO3
Reaction #66923
2-(1-Naphthalenyl)-6,7-methylenedioxyquinolin-4-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1cc2c(cc1NC(=O)c1coc3ccccc13)OCO2
Reaction #66924
N-(6-Acetyl-1,3-benzodioxol-5-yl)-1-benzofuran-3-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC(c2coc3ccccc23)=Nc2cc3c(cc21)OCO3
Reaction #66925
2-(3-Benzo[b]furyl)-6,7-methylenedioxyquinolin-4-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1cc2c(cc1NC(=O)c1cccc3ccccc13)OCO2
Reaction #66926
150
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC(c2cccc3ccccc23)=Nc2cc3c(cc21)OCO3
Reaction #66927
2-(1-Naphthalenyl)-6,7-methylenedioxyquinolin-4-one
Rendement 52.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1cc2c(cc1NC(=O)c1coc3ccccc13)OCO2
Reaction #66929
155
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC(c2coc3ccccc23)=Nc2cc3c(cc21)OCO3
Reaction #66930
2-(3-Benzo[b]furyl)-6,7-methylenedioxyquinolin-4-one
Rendement 17.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OCc2ccccc2)cc(C(=O)Nc2cc3c(cc2C(C)=O)OCO3)c1
Reaction #66936
164
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(O)cc(C2=Nc3cc4c(cc3C(=O)C2)OCO4)c1
Reaction #66938
166
Rendement 77.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1nc2ccc3ncnc(Nc4ccc5c(c4)OCO5)c3c2s1
Reaction #90389
9-(Benzo[d][1,3]dioxol-5-ylamino)thiazolo[5,4-f]quinazoline-2-carbonitrile
Rendement 49.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1nc2ccc3ncnc(Nc4ccc5c(c4Br)OCO5)c3c2s1
Reaction #90390
9-(4-Bromobenzo[d][1,3]dioxol-5-ylamino)thiazolo[5,4-f]quinazoline-2-carbonitrile
Rendement 21.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(NCc2ccccn2)nc(Nc2ccc3c(c2)OCO3)c1C
Reaction #91429
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
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