Substructure Search

1269374

C#CCn1c(=O)[nH]c(=O)n(-c2cc(N3C(=O)C4=C(CCCC4)C3=O)c(F)cc2Cl)c1=O
Reaction #1579
title product
Yield 55.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2=C(CCCC2)C(=O)N1c1ccc(Cl)cc1F
Reaction #1580
title product
Yield 69.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2CCCCC2C(=O)N1CCOCCO
Reaction #3164
N-(2-hydroxyethoxyethyl)hexahydrophthalimide
Yield 96.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CC(=O)OCC(CN1C(=O)C2CCCCC2C1=O)OC(=O)C=C
Reaction #3166
N-[2,3-di(hydroxy)propyl]hexahydrophthalimide
Yield 109.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CN1C(=O)C2=C(CCCC2)C1=O)C1(C)OCCO1
Reaction #10959
Ethyl 3-(1,3-dioxo-1,3,4,5,6,7-hexahydro-isoindol-2-yl)-2-(2-methyl-[1,3]dioxolan-2-yl)propionate
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2=C(CCCC2)C(=O)N1c1cc(OC2CCCC2)c(Cl)cc1F
Reaction #49741
N-(2-fluoro-4-chloro-5-cyclopentyloxyphenyl)-3,4,5,6-tetrahydrophthalimide
Yield 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CCCC1Oc1cc(N2C(=O)C3=C(CCCC3)C2=O)c(F)cc1Cl
Reaction #49744
N-{2-fluoro-4-chloro-5-(2-methylcyclopentyl)oxyphenyl}-3,4,5,6-tetrahydrophthalimide
Yield 98.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2=C(CCCC2)C(=O)N1c1cc(OC2CCCCC2)c(Cl)cc1F
Reaction #49745
N-(2-fluoro-4-chloro-5-cyclohexyloxyphenyl)-3,4,5,6-tetrahydrophthalimide
Yield 70.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)Oc1cc(N2C(=O)C3=C(CCCC3)C2=O)c(F)cc1Cl
Reaction #49756
N-(2-fluoro-4-chloro-5-methoxycarbonyloxyphenyl)-3,4,5,6-tetrahydrophthalimide
Yield 79.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2=C(CCCC2)C(=O)N1c1c(F)cc(Cl)c2nc(Cl)sc12
Reaction #50001
N-(2,4-Dichloro-6-fluorobenzothiazol-7-yl)-3,4,5,6-tetrahydrophthalimide
DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH][nH]c(=O)c2c1CCCC2
Reaction #70498
2,3,5,6,7,8-hexahydro-phthalazin-1,4-dione
Yield 96.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1C2CCC(O2)C1C(=O)OCc1ccccc1
Reaction #73454
10
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #75284
12.4
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2CCCCC2C(=O)N1c1ccc(Br)cc1F
Reaction #75286
2-(4-bromo-2-fluorophenyl)-3a,4,5,6,7,7a-hexahydro-1H-isoindole-1,3(2H)-dione
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(N2C(=O)C3CCCCC3C2=O)c(F)c1
Reaction #75288
4-(1,3-dioxo-2,3,3a,4,5,6,7,7a-octahydro-1H-isoindol-2-yl)-3-fluorobenzonitrile
DOI: 10.6084/m9.figshare.5104873.v1
C#CCn1c(=O)[nH]c(=O)n(-c2cc(N3C(=O)C4=C(CCCC4)C3=O)c(F)cc2Cl)c1=O
Reaction #80706
title product
Yield 55.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2=C(CCCC2)C(=O)N1c1ccc(Cl)cc1F
Reaction #80707
title product
Yield 69.3%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C1[C@H]2CCCC[C@H]2C(=O)N1CCCN1CCC(c2noc3cc(F)ccc23)CC1
Reaction #83900
cis-2-[3-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propyl]-hexahydro-1H-isoindole-1,3-dione hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C1[C@H]2CCCC[C@H]2C(=O)N1CCCCN1CCC(c2noc3cc(F)ccc23)CC1
Reaction #83902
cis-2-[4-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]butyl]hexahydro-1H-isoindole-1,3-dione hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
O=C1OC(=O)C2C3CCC(O3)C12
Reaction #155664
product
Yield 50.6%DOI: 10.6084/m9.figshare.5104873.v1
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