BOP

CON(C)C(=O)CCCc1c[nH]c2ccccc12
Reaction #979
amide
Выход 94.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(CC(=O)N[C@@H]1CCc2ccccc2NC1=O)NC(=O)OC(C)(C)C
Reaction #1832
product
Выход 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=O)NC1(c2ccccc2)CCN(CCOC(CN(C)C(=O)Cc2ccccc2)c2ccc(Cl)c(Cl)c2)CC1.CC(=O)NC1(c2ccccc2)CCN(CCOC(CN(C)C(=O)Cc2ccccc2)c2ccc(Cl)c(Cl)c2)CC1.Cl.Cl.O
Reaction #1939
hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)OC(=O)NC(C)(C)C(=O)N[C@H](CCc1ccccc1)C(=O)OCc1ccccc1
Reaction #2007
(R)-α-[(2-t-Butoxycarbonylamino-2-methyl-1-oxopropyl)amino]benzenebutanoic acid benzyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(CC(=O)N[C@H](CCc1ccccc1)C(=O)OCc1ccccc1)NC(=O)OC(C)(C)C
Reaction #2008
(R)-α-[(3-t-Butoxycarbonylamino-3-methyl-1-oxobutyl)amino]benzenebutanoic acid benzyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C=CCOC(=O)[C@@H](CCc1ccccc1)NC(=O)C(C)(C)NC(=O)OCc1ccccc1
Reaction #2011
desired product
Выход 69.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C=CCOC(=O)[C@@H](CCc1ccccc1)NC(=O)CC(C)(C)NC(=O)OCc1ccccc1
Reaction #2012
desired product
Выход 59.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C=CCOC(=O)[C@@H](CCc1ccccc1)NC(=O)CCC(C)(C)NC(=O)OCc1ccccc1
Reaction #2013
(R)-α-[(4-Benzyloxycarbonylamino-4-methyl-1-oxopentyl)amino]benzenebutanoic acid allyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C=CCOC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)C(C)(C)NC(=O)OCc1ccccc1
Reaction #2015
desired product
Выход 84.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1cc(C)cc(OC)c1NC(=O)CNC(=O)OC(C)(C)C
Reaction #3019
N-tert-butyloxycarbonyl-[(2,6-dimethoxy-4-methylphenyl)carbamoyl]methylamine
Выход 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)Cn1c(C(=O)NCC(=O)N(CCC(C)C)c2c(OC)cc(C)cc2OC)cc2ccccc21
Reaction #3020
methyl{2-[[(2,6-dimethoxy-4-methylphenyl)(isopentyl)carbamoyl]methylcarbamoyl]-1-indolyl}acetate
Выход 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1cc(C)cc(OC)c1N(CC1CCCCC1)C(=O)CNC(=O)c1cc2ccccc2n1CCC#N
Reaction #3021
3-{2-[[(cyclohexylmethyl)(2,6-dimethoxy-4-methylphenyl)carbamoyl]methylcarbamoyl]-1-indolyl}propionitrile
Выход 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)Cn1c(C(=O)N[C@H](CCCCNC(=O)C=Cc2ccccc2)C(=O)NCCCCCc2c(OC)cc(C)cc2OC)cc2ccccc21
Reaction #3024
methyl (R)-{2-[N-{1-[(2,6-dimethoxy-4-methylphenyl)pentylcarbamoyl]-5-(cinnamoylamino)pentyl}carbamoyl]indol-1-yl}acetate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(NCC1CC1)c1ccc(F)c(NCc2cnc(Nc3ccccn3)s2)c1
Reaction #6976
title compound
Выход 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(=O)OCc1ccccc1
Reaction #7767
acetic acid benzyl ester
Выход 215.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCn1cnc2c(Nc3ccc(NC(=O)c4cccc(Cl)c4)cc3)nc(NCCO)nc21
Reaction #10017
6-(4-[3-Chloro-benzoyl-amino]-phenyl-amino)-9-ethyl-2-(2-hydroxy-ethyl-amino)-9H-purine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(NCc1ccccc1)c1cc2nc(-c3ccc(Cl)c(Cl)c3)cc(C(F)(F)F)n2n1
Reaction #11978
5-(3,4-dichloro-phenyl)-7-trifluoromethyl-pyrazolo[1,5-a]pyrimidine-2-carboxylic acid benzylamide
Выход 89.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(NCc1ccccc1)c1cc2nc(-c3ccccn3)cc(C(F)(F)F)n2n1
Reaction #11979
5-pyridin-2-yl-7-trifluoromethyl-pyrazolo[1,5-a]pyrimidine-2-carboxylic acid benzylamide
Выход 86.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Nc1cc(-c2ccc(Cl)c(Cl)c2)nc2cc(C(=O)NCc3ccccc3)nn12
Reaction #11980
7-amino-5-(3,4-dichloro-phenyl)-pyrazolo[1,5-a]pyrimidine-2-carboxylic acid benzylamide
Выход 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(NCc1cccs1)c1cc2nc(-c3ccc(Br)cc3)cc(C(F)(F)F)n2n1
Reaction #11981
5-(4-bromo-phenyl)-7-trifluoromethyl-pyrazolo[1,5-a]pyrimidine-2-carboxylic acid (thiophen-2-ylmethyl)-amide
Выход 73.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
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