1-bromo-4-chlorobutane

CC(C)[N-]C(C)C.[Li+]
Reaction #1296
lithium diisopropylamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)[N-]C(C)C.[Li+]
Reaction #1432
lithium diisopropylamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
ClCCCCSc1ccccn1
Reaction #6268
desired compound
収率 65.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCC(=O)N(CCCCCl)c1ccccc1N(CCCCCl)C(=O)CC
Reaction #6282
desired product
収率 12.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
ClCCCCSc1ccncc1
Reaction #6286
desired compound
収率 89.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C1Nc2ccccc2C1=CNc1ccc(OCCCCCl)cc1
Reaction #11588
compound
収率 47.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1cn(CCCCCl)c(=O)[nH]c1=O
Reaction #40926
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(c1ccccc1)n1c(=O)c(I)cn(CCCCCl)c1=O
Reaction #40954
title compound
収率 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1nc(C)c(-c2cn(CCCCCl)c(=O)[nH]c2=O)o1
Reaction #40972
1-(4-Chloro-butyl)-5-(2,4-dimethyl-oxazol-5-yl)-1H-pyrimidine-2,4-dione
収率 47.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(c1ccccc1)n1c(=O)c(I)cn(CCCCCl)c1=O
Reaction #41026
title compound
収率 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)c1c2c(c(O)c(=O)n1CCCCCl)C(=O)N(Cc1ccc(F)c(Cl)c1)CC2
Reaction #46270
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C1OCCCCn2c1c1c(c(O)c2=O)C(=O)N(Cc2ccc(F)c(Cl)c2)CC1
Reaction #46308
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
ClCCCCc1ccco1
Reaction #49655
compound
収率 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
COC(=O)CSCCCCCl
Reaction #51240
[(4-chlorobutyl)thio]acetic acid methyl ester
収率 48.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1cccn(CCCCCl)c1=O
Reaction #176441
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
NC(=O)c1sc(-n2cnc3ccc(OCCCCCl)cc32)nc1-c1cccc(Cl)c1
Reaction #176754
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
ClCCCCSc1cccnc1
Reaction #178593
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
ClCCCCOc1ccccc1
Reaction #183402
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCC1(CCCCCl)C(=O)Nc2ccc(C)cc21
Reaction #184858
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C=CCn1c(-c2cccnc2)nn(CCCCCl)c1=O
Reaction #192237
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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