(3RS)-1-benzyl-3-chloromethyl pyrrolidine

ClCC1CCN(Cc2ccccc2)C1
Reaction #961
(3RS)-1-benzyl-3-chloromethyl pyrrolidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N#CCC1CCN(Cc2ccccc2)C1
Reaction #962
product
Rendement 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N#CCC1CCN(Cc2ccccc2)C1
Reaction #385965
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
ClCC1CCN(Cc2ccccc2)C1
Reaction #428987
(3RS)-1-benzyl-3-chloromethyl pyrrolidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
ClCC1CCN(Cc2ccccc2)C1
Reaction #783856
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
O=C(CC1CCN(Cc2ccccc2)C1)c1ccc(F)cc1F
Reaction #1325963
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
OC(CC1CCN(Cc2ccccc2)C1)c1ccc(F)cc1F
Reaction #1527999
expected product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_03
ClCC1CCN(Cc2ccccc2)C1
Reaction #1537891
(3RS)-1-benzyl-3-chloromethyl pyrrolidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_02
N#CCC1CCN(Cc2ccccc2)C1
Reaction #1537892
product
Rendement 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_02
ClCC1CCN(Cc2ccccc2)C1
Reaction #1672672
(3RS)-1-benzyl-3-chloromethyl pyrrolidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_08
N#CCC1CCN(Cc2ccccc2)C1
Reaction #1672673
product
Rendement 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_08
ClCC1CCN(Cc2ccccc2)C1
Reaction #1697989
(3RS)-1-benzyl-3-chloromethyl pyrrolidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_01
N#CCC1CCN(Cc2ccccc2)C1
Reaction #1697990
product
Rendement 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_01
ClCC1CCN(Cc2ccccc2)C1
Reaction #2043976
(3RS)-1-benzyl-3-chloromethyl pyrrolidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_07
N#CCC1CCN(Cc2ccccc2)C1
Reaction #2043977
product
Rendement 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_07
ClCC1CCN(Cc2ccccc2)C1
Reaction #2044328
(3RS)-1-benzyl-3-chloromethyl pyrrolidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_07
N#CCC1CCN(Cc2ccccc2)C1
Reaction #2044329
product
Rendement 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_07
O=c1[nH]c2ccccc2n1CC1CCN(Cc2ccccc2)C1
Reaction #2138867
1,3-dihydro-1-[1-(phenylmethyl)-3-pyrrolidinylmethyl]-2H-benzimidazol-2-one
Rendement 53.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_01
c1ccc(CN2CCC(CN3c4ccccc4CCc4ccccc43)C2)cc1
Reaction #2243752
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (4/10)
O=C(CC1CCN(Cc2ccccc2)C1)c1ccc(F)cc1F
Reaction #2313637
expected product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1994_09