5-chlorovaleryl chloride

COC(CN1CCCCC1=O)OC
Reaction #10279
1-(2,2-dimethoxyethyl)-piperidin-2-one
المردود 80.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(CCCCCl)Nc1ccc(N2C[C@H](CNC(=O)c3ccc(Cl)s3)OC2=O)cc1
Reaction #69368
5-Chloro-N-[((5S)-3-{4-[(5-chloropentanoyl)amino]phenyl}-2-oxo-1,3-oxazolidin-5-yl)methyl]-2-thiophenecarboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(CCCCCl)NC/C=C\COc1cc(CN2CCCCC2)ccn1
Reaction #80380
title compound
المردود 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=C(CCCCCl)Nc1ccc(N2C[C@H](CNC(=O)c3ccc(Cl)s3)OC2=O)cc1
Reaction #155660
5-Chloro-N-[((5S)-3-{4-[(5-chloropentanoyl)amino]phenyl}-2-oxo-1,3-oxazolidin-5-yl)methyl]-2-thiophenecarboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(CCCCCl)CS(=O)(=O)N1CCN(c2ccc(F)cc2)CC1
Reaction #180075
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CS(=O)(=O)NC1Cc2ccc(C(=O)CCCCCl)cc2C1
Reaction #186420
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(CCCCCl)Nc1cccc(-c2n[nH]c(=O)c3c2CCCC3)c1
Reaction #204278
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)c1cc(NC(=O)CCCCCl)cc(C(C)(C)C)c1O
Reaction #209870
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(CCCCCl)c1cc2c3c(c1)CCN3C(=O)CC2
Reaction #211924
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)[C@@H](NC(=O)CCCCCl)C(C)C
Reaction #216578
N-(5-chloropentanoyl)valine methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
N#CCCCCN(OCc1ccccc1)C(=O)CCCCCl
Reaction #222618
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ccc2oc(C(=O)CCCCCl)c(C)c2c1
Reaction #241623
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1nn(C)c(NC(=O)CCCCCl)c1C#N
Reaction #250276
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(CCCCCl)Nc1ccc(N2CC(CNC(=O)c3ccc(Cl)s3)OC2=O)cc1
Reaction #259716
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ccc(C(=O)CCCCCl)cc1
Reaction #262334
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)c1ccc(NC(=O)CCCCCl)c(Cl)c1
Reaction #271157
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOC(=O)Cc1ccccc1NC(=O)CCCCCl
Reaction #274305
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
N#CN1CCCCC1=O
Reaction #291330
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CN(CCc1ccccc1)C1CCN(C(=O)c2cccc(NC(=O)CCCCCl)c2)CC1
Reaction #297434
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
C[C@@H]([C@@H](O)c1ccccc1)N(C)C(=O)CCCCCl
Reaction #305608
5-chloro-N-((1S,2S)-1-hydroxy-1-phenylpropan-2-yl)-N-methylpentanamide
المردود 93.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
الصفحة 1التالي