部分構造検索

475

Clc1cccnc1NC1CCC1
Reaction #650
収率 25.0%
O=C1NCCC[C@H]1Nc1ncccc1Cl
Reaction #688
収率 2.0%
CN1CC(Nc2ncccc2Cl)CCC1=O
Reaction #722
収率 0.0%
CC1(CNc2ncccc2Cl)COC1
Reaction #736
収率 12.2%
CN1CC(Nc2ncccc2Cl)C1
Reaction #741
収率 0.0%
Clc1ccnc(Br)c1Cl
Reaction #48917
2-bromo-3,4-dichloropyridine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(Nc2cc(Cl)cnc2-c2ccccc2)c(C(=O)OC(C)(C)C)c1
Reaction #70343
tert-Butyl 2-(5-chloro-2-phenylpyridin-3-ylamino)-5-methylbenzoate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCC(=O)c1ncc(Cl)cc1Cl
Reaction #84294
desired product
収率 59.6%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)OC(C)(C)C)C(=O)c1ncc(Cl)cc1Cl
Reaction #84301
desired product
収率 65.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCC(=O)c1ncc(Cl)cc1Cl)c1ccccc1C(F)(F)F
Reaction #84312
desired product
収率 23.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc(-c2ncc(Br)cc2Cl)c(O[SiH](c2ccccc2)c2ccccc2)c1
Reaction #174805
DOI: 10.1039/C8SC04228D
Fc1cc(-c2nc(NCC3CCOCC3)c(Cl)cc2Cl)c(Cl)cn1
Reaction #180613
DOI: 10.1039/C8SC04228D
Fc1cc(-c2nc(NCC3CCOCC3)ccc2Cl)c(F)cn1
Reaction #237159
DOI: 10.1039/C8SC04228D
Fc1cc(-c2nc(NCC3CCOCC3)ccc2Cl)c(Cl)cn1
Reaction #255667
DOI: 10.1039/C8SC04228D
COC(=O)c1cc(S(=O)(=O)c2cnc(Br)c(Cl)c2)c(SC)s1
Reaction #274075
DOI: 10.1039/C8SC04228D
On1c(C(F)(F)F)nc2nc(Br)c(Cl)c(Br)c21
Reaction #287438
DOI: 10.1039/C8SC04228D
CC(C#N)c1ncccc1Cl
Reaction #295523
DOI: 10.1039/C8SC04228D
COC(=O)c1ccc(-c2ncc(Cl)cc2Cl)c(-c2ccc(Cl)c(OCc3ccc(OC)cc3)c2)n1
Reaction #331242
methyl 2′-[3-[(4-methoxybenzyl)oxy]-4-chlorophenyl]-3,5-dichloro-2,3′-bipyridine-6′-carboxylate
収率 38.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(-c2ncc(C)cc2Cl)c(-c2ccc(Cl)c(OCc3ccc(OC)cc3)c2)n1
Reaction #331249
methyl 3-chloro-2′-{4-chloro-3-[(4-methoxybenzyl)oxy]phenyl}-5-methyl-2,3′-bipyridine-6′-carboxylate
収率 64.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)C(=O)CN(c1ccc(C)cc1)S(=O)(=O)c1cnc(Br)c(Cl)c1
Reaction #378604
DOI: 10.1039/C8SC04228D
1 ページ次のページ