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11221

O=c1[nH]c2ccccc2c(=O)n1CCCSc1ccncc1
Reaction #6277
3-[3-(4-pyridylthio)propyl]quinazoline-2,4-(1H,3H)-dione
Ausbeute 31.1%DOI: 10.6084/m9.figshare.5104873.v1
O=c1c2ccccc2n(CCCCSc2ccccn2)c(=O)n1CCCCSc1ccccn1
Reaction #6278
desired product
Ausbeute 9.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(N2CC(C(C)N)C(C)(C)C2)c(F)cc2c(=O)n(N)c(=O)n(C3CC3)c12.Cl
Reaction #10403
3-Amino-7-[4-(1-aminoethyl)-3,3-dimethylpyrrolidin-1-yl]-1-cyclopropyl-6-fluoro-8-methyl-1H-quinazoline-2,4-dione hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)OC(C)(C)C)[C@H]1CCN(c2c(F)cc3c(=O)n(N(C)C(=O)OC(C)(C)C)c(=O)n(C4CC4)c3c2Cl)C1
Reaction #10405
title compound
Ausbeute 48.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)Nn1c(=O)c2cc(F)c(F)c(Cl)c2n(C2CC2)c1=O
Reaction #10407
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c2cc(F)c(F)cc2c(=O)n1N(Cc1ccccc1)Cc1ccccc1
Reaction #10409
title compound
Ausbeute 198.7%DOI: 10.6084/m9.figshare.5104873.v1
O=c1c2cc(F)c(F)cc2n(CC2CC2)c(=O)n1N(Cc1ccccc1)Cc1ccccc1
Reaction #10410
title compound
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CCn1c(=O)n(N(Cc2ccccc2)Cc2ccccc2)c(=O)c2cc(F)c(F)cc21
Reaction #10411
title compound
Ausbeute 73.3%DOI: 10.6084/m9.figshare.5104873.v1
Nn1c(=O)c2cc(F)c(F)cc2n(C2CC2)c1=O
Reaction #10423
3-amino-1-cyclopropyl-6,7-difluoro-1H-quinazoline-2,4-dione
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@H]1CCN(c2cc3c(cc2F)c(=O)n(N)c(=O)n3C2CC2)C1
Reaction #10424
title compound
Ausbeute 88.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)Nn1c(=O)c2cc(F)c(N3CCC(CNS(C)(=O)=O)C3)c(Cl)c2n(C2CC2)c1=O
Reaction #10439
{8-chloro-1-cyclopropyl-6-fluoro-7-[3-(methanesulfonylaminomethyl)pyrrolidin-1-yl]-2,4-dioxo-1,4-dihydro-2H-quinazolin-3-yl}carbamic acid tert-butyl ester
Ausbeute 8.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NS(=O)(=O)c1ccc(Cl)s1)c1ccc(-n2c(=O)[nH]c3ccccc3c2=O)cc1
Reaction #66421
desired compound
Ausbeute 34.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(-n2c(=O)[nH]c3ccccc3c2=O)c(Br)c1
Reaction #66440
desired compound
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c(=O)c2cc(I)ccc2[nH]1
Reaction #69045
6-iodoquinazolin-2,4(1H,3H)-dione
DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c(=O)c2cc(Cl)ccc2[nH]1
Reaction #73978
6-chloroquinazoline-2,4(1H,3H)-dione
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2ncnc(N3CCC(n4c(=O)c5cc([N+](=O)[O-])ccc5n(C)c4=O)CC3)c2cc1OC
Reaction #83283
Compound 1
Ausbeute 62.1%DOI: 10.6084/m9.figshare.5104873.v1
CCn1c(=O)n(C2CCN(c3ncnc4cc(OC)c(OC)cc34)CC2)c(=O)c2cc([N+](=O)[O-])ccc21
Reaction #83284
Compound 2
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCn1c(=O)n(C2CCN(c3ncnc4cc(OC)c(OC)cc34)CC2)c(=O)c2cc([N+](=O)[O-])ccc21
Reaction #83285
Compound 3
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCn1c(=O)n(C2CCN(c3ncnc4cc(OC)c(OC)cc34)CC2)c(=O)c2cc([N+](=O)[O-])ccc21
Reaction #83286
Compound 4
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCn1c(=O)n(C2CCN(c3ncnc4cc(OC)c(OC)cc34)CC2)c(=O)c2cc([N+](=O)[O-])ccc21
Reaction #83287
Compound 5
Ausbeute 53.0%DOI: 10.6084/m9.figshare.5104873.v1
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