dimethylaminopyridine

CCOC(=O)c1ccc(Cl)nc1
Reaction #1319
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC1(C)CCC(=O)c2ccc(C#Cc3ccc(C(=O)OCC[Si](C)(C)C)cc3)cc21
Reaction #1334
Trimethylsilylethyl 4-[(5,6,7,8-tetrahydro-8,8-dimethyl-5-oxonaphth-2-yl)ethynyl]benzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC1(C)CCC(=O)c2cc(C(=O)Oc3ccc(C(=O)OCc4ccccc4)cc3)ccc21
Reaction #1497
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN(C)Cc1ccc([C@H]2CC[C@@H](OC(=O)c3ccc(Cl)cc3)CC2)cc1
Reaction #1754
cis-O-(4-Chlorobenzoyl)-4-(4-dimethylaminomethylphenyl)-cyclohexanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=O)O[C@@H]1C=C[C@H](OC2CCCCO2)C1
Reaction #2654
title compound
収率 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1c(CC(=O)Nc2ccc(C(=O)N3Cc4cccn4Cc4ccccc43)cc2)sc2ccccc12
Reaction #3608
desired product
収率 39.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(CCl)Nc1ccc(C(=O)N2Cc3cccn3Cc3ccccc32)cc1
Reaction #3692
beige solid
収率 100.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1cc(NC(=O)c2ccccc2C)ccc1C(=O)N1CCCC(OC(=O)[C@H](CCSC)NC(=O)OC(C)(C)C)c2cc(Cl)ccc21
Reaction #5677
5-(N-tert-butoxycarbonyl-L-methionyloxy)-7-chloro-1-[2-methoxy-4-(2-methylbenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzazepine
収率 121.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Cc1ccccc1C(=O)Nc1ccc(C(=O)N2CCCC(OC(=O)[C@@H](N)C(C)C)c3cc(Cl)ccc32)c(C)c1
Reaction #5681
5-L-valyloxy-7-chloro-1-[2-methyl-4-(2-methylbenzoylamino)-benzoyl]-2,3,4,5-tetrahydro-1H-benzazepine
収率 38.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Cc1ccccc1C(=O)Nc1ccc(C(=O)N2CCCC(COC(=O)CN(C)C)c3cc(Cl)ccc32)cc1.Cl
Reaction #5683
5-[(2-dimethylaminoacetyloxy)methyl]-7-chloro-1-[4-(2-methylbenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzazepine hydrochloride
収率 141.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=S(=O)(Nc1ncccc1NCC=Cc1ccc(Cl)cc1)c1cccc2cnccc12
Reaction #5832
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCOC(=O)c1ccc(Cl)nc1
Reaction #6081
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCCCCCCCOc1ccc(OC(=O)c2ccc(OCCCCCC)cc2)c(F)c1F
Reaction #6427
2,3-difluoro-4-octyloxyphenyl 4-hexyloxybenzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCOC(=O)c1ccc(Cl)nc1
Reaction #6655
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCCCCC[C@@H](OC(=O)c1ccc(OC(=O)c2ccc(-c3ccc(OCCCCOCCCCC)c(F)c3F)cc2)cc1)C(F)(F)F
Reaction #6689
2′,3′-difluoro-4′-(4-pentyloxybutoxy)-biphenyl-4-carboxylic acid 4-[(R)-1-trifluoromethylheptyl oxycarbonyl]-phenyl ester
収率 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCCCCC[C@@H](OC(=O)c1ccc(OC(=O)c2ccc(-c3ccc(OCCCCOCCCCC)c(F)c3F)cc2)cc1)C(F)(F)F
Reaction #6695
2′,3′-difluoro-4′-(4-pentyloxybutoxy)-biphenyl-4-carboxylic acid 4-[(R)-1-trifluoromethylheptyloxycarbonyl]-phenyl ester
収率 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C=CC(=O)Nc1c(C)cccc1C(=O)NC(C)C
Reaction #7499
product
収率 52.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(=O)OCCOc1ccc(-c2nnnc(-c3cccc4ccccc34)c2-c2cccc3ccccc23)c(O)c1
Reaction #8442
bis-αnaphthyl-(4-[2-acetoxy-ethoxy]-2-hydroxy-phenyl)-triazine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)COc1ccc(Cl)cc1NS(=O)(=O)CC(=O)O
Reaction #11730
(5-Chloro-2-{2-[4-(4-fluoro-benzyl)-(2R,5S)-2,5-dimethyl-piperazin-1-yl]-2-oxo-ethoxy}-phenylsulfamoyl)-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C(=O)O)S(=O)(=O)NCc1cc(Cl)ccc1OCC(=O)N1C[C@H](C)N(Cc2ccc(F)cc2)C[C@H]1C
Reaction #11737
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
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