DMF

CCOC(=O)c1c[nH]c2c1C(=O)N(CC)CC2
Reaction #1003
ethyl 4-oxo-5-ethyl-4,5,6,7-tetrahydro-1H-pyrrolo[3,2-c]pyridine-3-carboxylate
収率 53.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)c1c(Br)[nH]c2c1C(=O)CCC2
Reaction #1005
2-bromo-4-oxo-4,5,6,7-tetrahydro-1H-indole-3-carboxylic acid
収率 29.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccncc1NC(=O)c1c[nH]c2c1C(=O)CCC2
Reaction #1006
N-(4-methoxy-3-pyridyl)-4-oxo-4,5,6,7-tetrahydro-1H-indole 3-carboxamide
収率 19.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1nc2n(c(=O)c1CCN1CCC(c3noc4cc(F)ccc34)CC1)CCCC2.O=C(O)c1cc2ccccc2c(Cc2c(O)c(C(=O)O)cc3ccccc23)c1O
Reaction #1007
3-[2-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]ethyl]-6,7,8,9-tetrahydro-2-methyl-4H-pyrido[1,2-a]pyrimidin-4-one 4,4'-methylenebis[3-hydroxy-2-naphthalenecarboxylate]
収率 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CSc1nccc(OCC(F)(F)F)n1
Reaction #1012
2-methylthio-4-(2,2,2-trifluoroethoxy)pyrimidine
収率 103.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccc(C=O)cc1OC1CCCC1
Reaction #1014
title compound
収率 89.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(N)COc1ccc(C#N)cc1
Reaction #1022
desired product
収率 41.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(N)COc1ccncc1
Reaction #1023
desired product
収率 30.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC#C[C@H](C)Oc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CCCOc2ccc(F)cc2)C[C@H]1OC
Reaction #1031
title compound
収率 91.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)CC(F)(Cl)C(F)(F)Br
Reaction #1036
4-bromo-3-chloro-3,4,4-trifiuorobutanoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(Cl)CC(F)=C(F)F
Reaction #1037
3,4,4-trifluoro-3-butenoyl chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)CC(F)(Cl)C(F)(F)Cl
Reaction #1040
compound XI
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N#CCN1CCC(c2ccc(Oc3ccccc3)cc2)CC1
Reaction #1062
compound ( 26 )
収率 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1ccc([N+](=O)[O-])cc1S(=O)(=O)O
Reaction #1091
2-methoxycarbonyl-5-nitrobenzenesulfonic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1ccc(NC=O)cc1S(=O)(=O)NC(C)(C)C
Reaction #1094
N-tert-Butyl-5-formylamino-2-methoxycarbonylbenzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)NC(=S)CNc1ccc(C(=O)OC)c(S(=O)(=O)NC(C)(C)C)c1
Reaction #1095
N-tert-butyl-5-[N-(ethoxycarbonylaminothiocarbonyl)methylamino]-2-methoxycarbonylbenzenesulfonamide
収率 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1nccc(N[C@H]2CC[C@@H](c3ccccc3)CC2)c1Br
Reaction #1124
2-Methoxy-3-bromo-4-(cis-4-phenylcyclohexylamino)pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N#Cc1ccc(NCC(O)CO)cc1
Reaction #1125
p-(N-2,3-dihydroxypropylamino)benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)[Si](C)(Cc1ccc(Br)cc1)O[Si](C)(Cc1ccc(Br)cc1)C(C)(C)C
Reaction #1133
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1oc(-c2ccccc2)nc1COc1ccc2cc(CCc3nnn[nH]3)oc2c1
Reaction #1144
5-[2-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranyl]ethyl ]-1H-tetrazole
収率 78.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
前のページ2 ページ次のページ