部分構造検索

10978

CC(C)(C)OC(=O)N1CCC(OS(C)(=O)=O)CC1
Reaction #6183
desired compound
収率 98.7%DOI: 10.6084/m9.figshare.5104873.v1
COC1(C(C)=O)CCN(C(=O)OC(C)(C)C)CC1
Reaction #8851
title compound
収率 37.1%DOI: 10.6084/m9.figshare.5104873.v1
CCC(O)CC(=O)C1(OC)CCN(C(=O)OC(C)(C)C)CC1
Reaction #8852
title compound
収率 55.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(O)(c2cc(C(F)(F)F)ccc2Sc2ccc(Cl)cc2)CC1
Reaction #43507
compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(O)(c2cc(F)ccc2Sc2cccc(Cl)c2)CC1
Reaction #43508
1-tert-Butoxycarbonyl-4-[2-(3-chloro-phenylsulfanyl)-5-fluoro-phenyl]-piperidine-4-ol
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(O)(c2cc(F)ccc2Sc2cccc(F)c2)CC1
Reaction #43509
1-tert-Butoxycarbonyl-4-[2-(3-fluoro-phenylsulfanyl)-5-fluoro-phenyl]-piperidine-4-ol
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(c2cc(C(F)(F)F)ccc2Sc2ccc(Cl)cc2)CC1
Reaction #43514
4-[2-(4-chloro-phenylsulfanyl)-5-trifluoromethyl-phenyl]-piperidine-1-carboxylic acid tert-butyl ester
収率 82.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(O)(c2cc3c(Br)ccnc3n2S(=O)(=O)c2ccccc2)CC1
Reaction #57277
title compound
収率 85.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc(-c2ccnc3c2cc(C2(O)CCN(C(=O)OC(C)(C)C)CC2)n3S(=O)(=O)c2ccccc2)c(-c2ccc([N+](=O)[O-])cc2)n1
Reaction #57278
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(Oc2nn(-c3ccccc3F)c3cccc(F)c23)CC1
Reaction #58691
Intermediate 46
収率 51.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(O)(CN)CC1
Reaction #72975
tert-butyl 4-(aminomethyl)-4-hydroxypiperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(O)(CNc2c([N+](=O)[O-])cnc3cccnc23)CC1
Reaction #73051
tert-butyl 4-hydroxy-4-{[(3-nitro[1,5]naphthyridin-4-yl)amino]methyl}piperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(O)(c2ccc(Cl)c(F)c2)CC1
Reaction #73836
title compound
収率 30.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC2(CC1)CO2
Reaction #75588
tert-butyl 1-oxa-6-azaspiro[2.5]octane-6-carboxylate
収率 83.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(O)(Cn2ccnc2)CC1
Reaction #75589
tert-butyl 4-hydroxy-4-(1H-1-imidazolylmethyl)-1-piperidinecarboxylate
収率 87.9%DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1(O)CCN(C(=O)OC(C)(C)C)CC1
Reaction #75600
tert-butyl 4-allyl-4-hydroxy-1-piperidinecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(O)(CC(O)CO)CC1
Reaction #75601
tert-butyl 4-(2,3-dihydroxypropyl)-4-hydroxy-1-piperidinecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(OS(C)(=O)=O)CC1
Reaction #85857
tert-butyl4-(methylsulfonyloxy)piperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(n2cc(B3OC(C)(C)C(C)(C)O3)cn2)CC1
Reaction #85858
crude pale yellow oil
収率 117.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cncc(-c2cc3c(cn2)cnn3-c2cccc(C3CN(C(=O)OC(C)(C)C)CCC3O)n2)n1
Reaction #86267
desired product
収率 45.6%DOI: 10.6084/m9.figshare.5104873.v1
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