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765393

Cc1cc(Cl)nc2c1CNCC2.Cl
Reaction #168004
2-chloro-4-methyl-5,6,7,8-tetrahydro-1,6-naphthyridine hydrochloride
Ausbeute 179.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C(C)C)cc1O
Reaction #168005
Carvacrol
Ausbeute 48.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Cl)nc2c1CN(C(=O)CC(=O)C1CC1)CC2
Reaction #168008
1-(2-chloro-4-methyl-7,8-dihydro-1,6-naphthyridin-6(5H)-yl)-3-cyclopropylpropane-1,3-dione
Ausbeute 52.4%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cccc(CC)c1-c1cc(C)c2c(n1)CCN(c1nnnn1C)C2
Reaction #168010
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc2c(nc1Cl)CCNC2.Cl
Reaction #220016
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(OC(C)(C)C)c1c(C)nc2c(c1-c1ccc(C)cc1)CNCC2.Cl.Cl
Reaction #558111
methyl 2-(tert-butoxy)-2-(2-methyl-4-(p-tolyl)-5,6,7,8-tetrahydro-1,6-naphthyridin-3-yl)acetate 2 HCl
DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc2c(cc1C(=O)OCC)C(=O)N(C1CCNCC1)CC2.Cl.Cl.O
Reaction #618273
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc2c(cc1C(=O)OCC)C(=O)N(C1CCN(Cc3cc(C4CC4)c(-c4ccc(F)cc4)c(F)c3OCC)CC1)CC2
Reaction #618274
title compound
Ausbeute 93.1%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nc2c(cc1C(=O)OC)C(=O)N(C1CCNCC1)CC2.Cl.Cl
Reaction #618285
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCc1nc2c(cc1C(=O)OC)C(=O)N(C1CCN(Cc3cc(C4CC4)c(-c4ccc(F)cc4)c(F)c3OC(C)C)CC1)CC2
Reaction #618286
title compound
Ausbeute 73.3%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nc2c(cc1C(=O)OC)C(=O)N(C1CCNCC1)CC2.Cl.Cl
Reaction #618296
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1c(CN2CCC(N3CCc4nc(CC)c(C(=O)OC)cc4C3=O)CC2)cc(C2CC2)c(-c2ccc(F)cc2)c1F
Reaction #618297
title compound
Ausbeute 62.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc2c(cc1C(=O)OCC)C(=O)N(C1CCNCC1)CC2.Cl.Cl.O
Reaction #618329
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc2c(cc1C(=O)OCC)C(=O)N(C1CCN(Cc3cc(C4CC4)c(-c4ccc(F)cc4F)cc3OCC)CC1)CC2
Reaction #618330
title compound
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2nc(N3CCc4ncccc4C3)sc2c(-c2ccc(Cl)cc2)c1[C@H](OC(C)(C)C)C(=O)O
Reaction #966586
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@]1(C(=O)N2CCc3ncc(C(F)(F)F)cc3C2)CC[C@@H](NC(=O)OC(C)(C)C)C1
Reaction #1056761
desired product
Ausbeute 114.7%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #1132540
product
Ausbeute 33.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCc2nc3ccc(Cl)cc3c(Oc3ccccc3)c2C1
Reaction #1281875
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCc2nc3ccc(Cl)cc3c(Nc3ccccc3)c2C1
Reaction #1281876
10-Anilino-8-chloro-1,2,3,4-tetrahydro-2-methylbenzo[b][1,6]naphthyridine
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCc2nc3ccc(Cl)cc3c(SCCCN)c2C1
Reaction #1281877
title compound
Ausbeute 53.0%DOI: 10.6084/m9.figshare.5104873.v1
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