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13099

CC(C)(C)OC(=O)N(CCF)C1CCNC1
Reaction #1981
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1(C(F)(F)F)CCN(Cc2ccccc2)C1
Reaction #1983
title compound
Ausbeute 96.7%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N#Cc1cccc(CN2CC[C@H](N)C2=O)c1
Reaction #2841
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H]1CCN(c2ccc(N)cc2F)C1
Reaction #8266
required product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(F)cc(N2CC[C@H](NC(=O)OC(C)(C)C)C2)c(F)c1NC1CC1
Reaction #10385
title compound
Ausbeute 81.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(N2CCC(NC(=O)OC(C)(C)C)C2)c(F)c1NC1CC1
Reaction #10390
title compound
Ausbeute 76.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(Cl)c(N2CCC(NC(=O)OC(C)(C)C)C2)c(F)c1NC1CC1
Reaction #10391
title compound
Ausbeute 48.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1CCN(c2ccc(C(=O)O)c(NC3CC3)c2F)C1
Reaction #10394
title compound
Ausbeute 112.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1CCN(c2c(Cl)cc(C(=O)O)c(NC3CC3)c2F)C1
Reaction #10395
title compound
Ausbeute 91.3%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
Ausbeute 86.8%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
Ausbeute 76.0%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
Ausbeute 71.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(NC(=O)c2ccc(CN3CC[C@H](NC(=O)OC(C)(C)C)C3=O)c(C(F)(F)F)c2)cc1Nc1nccc(-c2cncnc2)n1
Reaction #42071
objective compound
DOI: 10.6084/m9.figshare.5104873.v1
CN[C@H]1CCN(C2CCCCC2(O)C(C)c2cccc(C(F)(F)F)c2)C1.Cl.Cl
Reaction #57103
2-[(3S)-3-(methylamino)pyrrolidin-1-yl]-1-[3-(trifluoromethyl)phenyl]ethylcyclohexanol Dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@H]1CN(C(C)(C)C)[C@](C[C@@H](O)[C@@H](N)Cc2ccccc2)(C(N)=O)C1.N#N
Reaction #82391
N2 [3(S)-amino-2(R)-hydroxy-4-phenylbutyl]-4(R)-(tert.butoxyformamido)-N1 -tert.butyl-L-prolinamide
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN(C(=O)OC(C)(C)C)[C@H]1CCN(c2c(Br)cnc3c2c2cc(C#N)ncc2n3COCC[Si](C)(C)C)C1
Reaction #88555
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN[C@H]1CCN(c2c(Br)cnc3[nH]c4cnc(C#N)cc4c23)C1
Reaction #88556
title compound
Ausbeute 59.7%DOI: 10.6084/m9.figshare.5104873.v1
CCN(C(=O)OC(C)(C)C)[C@H]1CCN(c2c(F)cnc3c2c2cc(C#N)ncc2n3COCC[Si](C)(C)C)C1
Reaction #88557
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN[C@H]1CCN(c2c(F)cnc3[nH]c4cnc(C#N)cc4c23)C1
Reaction #88558
title compound
Ausbeute 77.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@H]1CCN(C(=O)OCc2ccccc2)C1
Reaction #88585
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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