Substructure Search

CC(C)(C)OC(=O)N=NC(=O)OC(C)(C)C

COC(=O)[C@@H]1C[C@H](OC(C)=O)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@H](c3ccoc3)C[C@]21C
Reaction #40598
34
Yield 81.6%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C(=O)N(C2CCCCCC2)CC1COc1ccccc1
Reaction #44485
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc2cc(OC3CCN(C(C)C)CC3)ccc2[nH]1
Reaction #48118
desired product
Yield 66.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1OC1CCOCC1
Reaction #57440
2-(tetrahydro-2H-pyran-4-yloxy)-1H-isoindole-1,3(2H)-dione
DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1OC1CCCCC1
Reaction #57478
2-(cyclohexyloxy)-1H-isoindole-1,3(2H)-dione
Yield 75.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(OCCCN2CCCCC2)no1
Reaction #58762
product
Yield 192.6%DOI: 10.6084/m9.figshare.5104873.v1
ClCCl.N
Reaction #61996
ammonia DCM
Yield 2.5%DOI: 10.6084/m9.figshare.5104873.v1
ClCCl.N
Reaction #62002
ammonia DCM
Yield 3.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc(-c2cc(F)c3nnc(C(F)(F)c4ccc5ncc(OCCCN6CCOCC6)cc5c4)n3c2)cn1
Reaction #68628
6-(difluoro(8-fluoro-6-(1-methyl-1H-pyrazol-4-yl)-[1,2,4]triazolo[4,3-a]pyridin-3-yl)methyl)-3-(3-morpholinopropoxy)quinoline
Yield 33.0%DOI: 10.6084/m9.figshare.5104873.v1
COCCOc1cnc2ccc(CC(=O)OC(C)(C)C)cc2c1
Reaction #68629
tert-butyl 2-(3-(2-methoxyethoxy)quinolin-6-yl)acetate
Yield 82.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(OC2CN(c3ccc([C@H](C)NC(C)=O)cc3)C2)n1
Reaction #68807
desired product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccccc1)N1CCN(Cc2ccc(OC3CCCCC3)cc2)CC1
Reaction #68869
title compound
Yield 28.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2cc(F)c(CN3C(=O)CSC3=O)cc2C1=Cc1cc(CN2CCOCC2)c[nH]1
Reaction #72580
title product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(N(NC(=O)OC(C)(C)C)C(=O)OC(C)(C)C)CCN(Cc2ccccc2)CC1
Reaction #92582
crude product
Yield 73.3%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.Cl.O=c1[nH]ccc2cc(OCCCN(CCc3cccnc3)Cc3ccncc3)ccc12
Reaction #156189
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NN(CC1CCC(F)(F)CC1)C(=O)OC(C)(C)C
Reaction #156304
di-tert-butyl 1-[(4,4-difluorocyclohexyl)methyl]hydrazine-1,2-dicarboxylate
Yield 113.1%DOI: 10.6084/m9.figshare.5104873.v1
CN1CC[C@H](NN)C1.Cl.Cl
Reaction #156306
(3S)-3-hydrazino-1-methylpyrrolidine dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)Nc1nnc(CSc2ccc(Cl)cc2N)[nH]1
Reaction #157548
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(Cl)ccc1SCCc1cn[nH]c1
Reaction #157552
title intermediate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)O[C@@H]1C[C@H](OC(=O)c2ccccc2)CN(C(=O)OCc2ccccc2)C1
Reaction #160707
(3S,5R)-benzyl 3-(benzoyloxy)-5-(tert-butyl-dimethylsilyloxy)piperidine-1-carboxylate
Yield 77.0%DOI: 10.6084/m9.figshare.5104873.v1
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