phthalimide

O=C(OCc1ccccc1)N1CCC(N2C(=O)c3ccccc3C2=O)CC1
Reaction #1173
1-benzyloxycarbonyl-4-phthalimidylpiperidine
Ausbeute 50.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccccc1NC(=O)c1ccc(CN2C(=O)c3ccccc3C2=O)cc1
Reaction #2548
title compound
Ausbeute 77.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1ccccc1-c1ccc(CN2C(=O)c3ccccc3C2=O)cc1
Reaction #5957
title compound
Ausbeute 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
COCC1(CN2C(=O)c3ccccc3C2=O)CCN(Cc2ccccc2)C1
Reaction #10454
title compound
Ausbeute 21.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C1c2ccccc2C(=O)N1C[C@H]1CO1
Reaction #40656
desired product
Ausbeute 73.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C1c2ccccc2C(=O)N1CC1Cc2ccc3c(c2O1)CCC3
Reaction #42234
(±)-2-(3,6,7,8-tetrahydro-2H-indeno[4,5-b]furan-2-ylmethyl)-1H-isoindole-1,3(2H)-dione
Ausbeute 77.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C1c2ccccc2C(=O)N1Cc1cccc(Br)n1
Reaction #45378
2-((6-Bromopyridin-2-yl)methyl)isoindoline-1,3-dione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C1c2ccccc2C(=O)N1[C@@H]1C=Cc2ccccc2[C@H]1O
Reaction #57072
2
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C1c2ccccc2C(=O)N1Cc1cccc(Br)n1
Reaction #57537
2-(6-Bromo-pyridin-2-ylmethyl)-isoindole-1,3-dione
Ausbeute 80.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C(CN1C(=O)c2ccccc2C1=O)c1ccc(Cl)cc1Cl
Reaction #60042
2-[2-(2,4-dichlorophenyl)-2-oxoethyl]isoindoline-1,3-dione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C(CN1C(=O)c2ccccc2C1=O)c1ccc(Cl)cc1Cl
Reaction #60048
2-[2-(2,4-dichlorophenyl)-2-oxoethyl]isoindoline-1,3-dione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C(CN1C(=O)c2ccccc2C1=O)c1ccc(Cl)cc1Cl
Reaction #60067
2-[2-(2,4-dichlorophenyl)-2-oxoethyl]isoindoline-1,3-dione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C(CN1C(=O)c2ccccc2C1=O)c1ccc(Cl)cc1Cl
Reaction #60072
2-[2-(2,4-dichlorophenyl)-2-oxoethyl]isoindoline-1,3-dione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C(CN1C(=O)c2ccccc2C1=O)c1ccc(Cl)cc1Cl
Reaction #60077
2-[2-(2,4-dichlorophenyl)-2-oxoethyl]isoindoline-1,3-dione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C(CN1C(=O)c2ccccc2C1=O)c1ccc(Cl)cc1Cl
Reaction #60082
2-[2-(2,4-dichlorophenyl)-2-oxoethyl]isoindoline-1,3-dione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C(CN1C(=O)c2ccccc2C1=O)c1ccc(Cl)cc1Cl
Reaction #60091
2-[2-(2,4-dichlorophenyl)-2-oxoethyl]isoindoline-1,3-dione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C(CN1C(=O)c2ccccc2C1=O)c1ccc(Cl)cc1Cl
Reaction #60127
2-[2-(2,4-dichlorophenyl)-2-oxoethyl]isoindoline-1,3-dione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C(CN1C(=O)c2ccccc2C1=O)c1ccc(Cl)cc1Cl
Reaction #60218
2-[2-(2,4-dichlorophenyl)-2-oxoethyl]isoindoline-1,3-dione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C(CN1C(=O)c2ccccc2C1=O)c1ccc(Cl)cc1Cl
Reaction #60227
2-[2-(2,4-dichlorophenyl)-2-oxoethyl]isoindoline-1,3-dione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C1c2ccccc2C(=O)N1C/C=C\COC1CCCCO1
Reaction #64858
title compound
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
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