Recherche de Sous-structure

14323

O=c1[nH]cnc2cc(I)ccc12
Reaction #6915
title compound
Rendement 17.8%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N[C@@H]1CN(c2c(F)cc3c(=O)n(N)c(=O)n(C4CC4)c3c2Cl)C[C@H]1c1ccc(O)cc1
Reaction #10402
3-Amino-7-[trans-3-amino-4-(4-hydroxyphenyl)pyrrolidin-1-yl]-8-chloro-1-cyclopropyl-6-fluoro-1H-quinazoline-2,4-dione hydrochloride
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
CC(C)(C)OC(=O)N[C@H]1CCN(c2c(F)c(NCc3ccccc3)c3c(=O)n(NC(=O)OC(C)(C)C)c(=O)n(C4CC4)c3c2F)C1
Reaction #10404
{7-[(S)-3-(tert-butoxycarbonylamino)pyrrolidin-1-yl]-5-benzylamino-1-cyclopropyl-6,8-difluoro-1,4-dihydro-2,4-dioxo-2H-quinazolin-3-yl}carbamic acid tert-butyl ester
Rendement 86.8%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
Rendement 48.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@H]1CCN(c2c(F)c(N)c3c(=O)n(NC(=O)OC(C)(C)C)c(=O)n(C4CC4)c3c2F)C1
Reaction #10406
{5-amino-7-[(S)-3-(tert-butoxycarbonylamino)pyrrolidin-1-yl]-1-cyclopropyl-6,8-difluoro-1,4-dihydro-2,4-dioxo-2H-quinazolin-3-yl}-carbamic acid tert-butyl ester
Rendement 76.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(N2CC[C@H]([C@@H](C)NC(=O)OC(C)(C)C)C2)c(F)cc2c(=O)n(N)c(=O)n(C3CC3)c12
Reaction #10426
title compound
Rendement 96.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(N2CC[C@H]([C@@H](C)NC(=O)OC(C)(C)C)C2)c(F)cc2c(=O)n(N)c(=O)n(C3CC3)c12
Reaction #10427
title compound
Rendement 45.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(N2CC[C@H]([C@H](C)NC(=O)OC(C)(C)C)C2)c(F)cc2c(=O)n(N)c(=O)n(C3CC3)c12
Reaction #10428
title compound
Rendement 52.5%DOI: 10.6084/m9.figshare.5104873.v1
CC1CCc2c(N3CC[C@H](NC(=O)OC(C)(C)C)C3)c(F)cc3c(=O)n(N)c(=O)n1c23
Reaction #10431
title compound
Rendement 71.8%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
Rendement 8.4%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]cnc2cc(I)ccc12
Reaction #79409
title compound
Rendement 17.8%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)Nn1c(=O)[nH]c2cc([N+](=O)[O-])c(NCCOCc3ccccc3)cc2c1=O
Reaction #192142
DOI: 10.1039/C8SC04228D
CC1C(N=C(Nc2ccc3c(=O)n(CCc4ccc(F)cc4)cnc3c2)N2CC(N)C2)CC2CC1C2(C)C
Reaction #196826
DOI: 10.1039/C8SC04228D
CS(=O)(=O)Nn1c(=O)[nH]c2cc([N+](=O)[O-])c(-n3ccnn3)cc2c1=O
Reaction #198994
DOI: 10.1039/C8SC04228D
CS(=O)(=O)Nn1c(=O)[nH]c2cc([N+](=O)[O-])c(NC(CO)Cc3c[nH]cn3)cc2c1=O
Reaction #199131
DOI: 10.1039/C8SC04228D
Nc1ccc2c(=O)[nH]cnc2c1
Reaction #201222
DOI: 10.1039/C8SC04228D
CCn1c(=O)n(O)c(=O)c2cc(F)c(N3CCCCC3)cc21
Reaction #202700
DOI: 10.1039/C8SC04228D
CC(=O)Nc1ccc2c(=O)n(CCCCN3CCC(C(=O)c4ccc(F)cc4)CC3)c(=O)[nH]c2c1
Reaction #205929
DOI: 10.1039/C8SC04228D
CCn1c(=O)n(O)c(=O)c2cc(F)c(N3CCNCC3)cc21
Reaction #221404
DOI: 10.1039/C8SC04228D
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