benzyloxy acetyl chloride

NS(=O)(=O)c1ccc(CCN(Cc2cccc(-c3cccc(C(=O)NCCN4CCCC4)c3)c2)C(=O)COCc2ccccc2)cc1
Reaction #9873
3′-{({2-[4-(Aminosulfonyl)phenyl]ethyl}[(benzyloxy)acetyl]amino)methyl}-N-[2-(1-pyrrolidinyl)ethyl][1,1′-biphenyl]-3-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C1CCC(N2C(=O)c3cccc(NC(=O)COCc4ccccc4)c3C2=O)C(=O)N1
Reaction #10090
product
Ausbeute 80.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(COCc1ccccc1)Oc1cccc2c1C(=O)c1c(OC(=O)COCc3ccccc3)cc(C(=O)O)cc1C2=O
Reaction #41218
4,5-Bis(2-benzyloxyacetyloxy)-9,10-dioxo-9,10-dihydroanthracene-2-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1c(C#N)c(NC(=O)COCc2ccccc2)c(O)c(F)c1-c1ccccc1
Reaction #45624
compound
Ausbeute 77.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccc(CCNC(=O)COCc2ccccc2)cc1OC
Reaction #76860
N-[2-(3,4-Dimethoxy-phenyl)-ethyl]-benzyloxy-acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CCCOc1ccc(F)c2c(=O)c(-c3ccc(OC)cc3)cn(C(=O)COCc3ccccc3)c12
Reaction #155355
1-(2-benzyloxyacetyl)-5-fluoro -3-(4-methoxyphenyl)-8-propoxy-1H-quinolin-4-one
Ausbeute 15.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(O)c1ccc2c(c1)nc(COCc1ccccc1)n2-c1ccccc1
Reaction #161336
title compound
Ausbeute 86.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)C(C)Oc1ccc(NC(=O)COCc2ccccc2)cc1
Reaction #170997
51
Ausbeute 59.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)CCCCCOc1ccc(NC(=O)COCc2ccccc2)cc1
Reaction #170999
53
Ausbeute 22.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CN(C(=O)c1cc2c(s1)-c1ccc(NC(=O)CO)cc1OCC2)c1ccccc1Cl
Reaction #171643
158
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)C1C(OCc2ccccc2)C(=O)N1c1ccc(OC)cc1
Reaction #181394
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)c1ccc(Cl)c(NC(=O)COCc2ccccc2)c1
Reaction #196346
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)C(C)Oc1ccc(NC(=O)COCc2ccccc2)cc1
Reaction #196576
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)C(=O)CN(C)C(=O)COCc1ccccc1
Reaction #198863
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)CNC(=O)COCc1ccccc1
Reaction #206873
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(COCc1ccccc1)NC1CC(n2cnc3c(NCC(c4ccccc4)c4ccccc4)nc(Cl)nc32)C(O)C1O
Reaction #209298
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc([N+](=O)[O-])c(OC(=O)COCc2ccccc2)c(OC)c1OC
Reaction #213262
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)C(C)Oc1ccc(NC(=O)COCc2ccccc2)cc1
Reaction #231588
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(C)[Si](C)(C)Oc1ccc2c(c1)CCC(c1ccc(O[Si](C)(C)C(C)(C)C)cc1N(CCOCc1ccccc1)Cc1ccc(OCCN3CCCCCC3)cc1)C2
Reaction #231894
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(C)OC(=O)NCC1CN(c2ccc3c(c2)CCN(C(=O)COCc2ccccc2)C3)C(=O)O1
Reaction #243775
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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