formic acid

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
COc1c(NC2CCC(=O)CC2)ccnc1C.Cl
Reaction #1101
4-(4-Oxocyclohexylamino)-3-methoxy-2-methylpyridine hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1c(OC2CCC(=O)CC2)ccnc1C
Reaction #1112
4-(4-Oxocyclohexyloxy)-3-methoxy-2-methylpyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN1CCCC1c1cncc(Br)c1
Reaction #1143
5-bromo-3-(1-methyl-2-pyrrolidinyl)pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
c1ccc2c(c1)OC(c1ccc(OCCN3CCCCC3)cc1)c1c-2sc2ccccc12
Reaction #1804
title compound
Ausbeute 57.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cl.O=C(O)CNC(=O)c1nc2ccc(OCC(F)(F)F)cc2cc1O
Reaction #1837
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1ccc(C2CCCN2C)cn1
Reaction #1857
XVII
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=CNNC(=O)Nc1ccccc1
Reaction #2423
1-formyl-4-phenylsemicarbazide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=CNc1cccc(C(=O)O)c1
Reaction #2428
3-(Formylamino)benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=c1cc(O)cc(C=Cc2ccc(O)c(O)c2)o1
Reaction #3008
6-[2-(3,4-Dihydroxyphenyl)vinyl]-4-hydroxy-2H-pyran-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1cc(C)cc(OC)c1NC1C2CC3CC(C2)CC1C3
Reaction #3016
N-(2-adamantyl)-2,6-dimethoxy-4-methylaniline
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)[C@H](Cc1ccccc1)NC=O
Reaction #3064
N-formylphenylalanine methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
—
Reaction #3141
hydrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CNc1nc(N)ncc1C=O
Reaction #3258
2-amino-4-methylamino-5-pyrimidinecarboxaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CNc1nc(SC)ncc1C=O
Reaction #3263
4-Methylamino-2-methylsulfanyl-pyrimidine-5-carboxaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Nc1ccnc(N)c1C=O
Reaction #3512
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Nc1nc(Nc2ccccc2)ncc1C=O
Reaction #3542
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=c1c2[nH]cnc2n(CC2CC2)c(=O)n1CC1CC1
Reaction #3739
1,3-Di-cyclopropylmethyl xanthine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)[C@@H]1CCCC2c3ccccc3CC(N3C(=O)c4ccccc4C3=O)C(=O)N21
Reaction #3773
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)[C@@H]1CCCC2c3ccccc3CC(N3C(=O)c4ccccc4C3=O)C(=O)N21
Reaction #3774
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
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