2-bromo propionyl bromide

COc1cccc(N(C)C(=O)C(C)Br)c1
Reaction #1863
2-Bromo-N-(3-methoxyphenyl)-N-methyl-propanamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)COC(=O)C(C)Br
Reaction #51299
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CC(Br)C(=O)NCCS(=O)(=O)[O-].[Na+]
Reaction #52577
Sodium 2-(2-bromopropionylamino)-ethanesulfonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CC(Br)C(=O)c1ccc2c(c1)CN(C)C(=O)N2
Reaction #63180
6-(2-bromopropionyl)-3,4,dihydro-3-methyl-2(1H)-quinazolinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
CC[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)CC[C@@H]4[C@H]3CC[C@]2(C)[C@H]1OC(=O)C(C)Br
Reaction #92983
above-identified compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
CC(Br)C(=O)OCCSCc1ccccc1
Reaction #93668
2-benzylthioethyl 2-bromopropionate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
COc1cccc(N(C)C(=O)C(C)Br)c1
Reaction #190405
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(Br)C(=O)N1C(=O)N(C)C(C)(C)C1(C)C
Reaction #194548
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCC1CC2C3CCC4=CC(=O)CCC4C3CCC2(C)C1OC(=O)C(C)Br
Reaction #207585
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(Br)C(=O)OC(C)(C)C
Reaction #208018
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(Br)C(=O)N(C)C#N
Reaction #209149
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)N1CCc2c(sc(NC(=O)C(C)Br)c2C(=O)c2ccccc2Cl)C1
Reaction #216673
intended product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
C#CCCOC(=O)N1CCc2c(sc(NC(=O)C(C)Br)c2C(=O)c2ccccc2Cl)C1
Reaction #216680
intended compound
المردود 65.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
CC(Br)C(=O)Nc1sc2c(c1C(=O)c1ccccc1Cl)CCN(C(=O)C1CC1)C2
Reaction #216685
intended compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
CC(Br)C(=O)CNc1c(I)c(C(=O)O)c(I)c(C(=O)N(CCNC(=O)C(C)Br)CCNC(=O)C(C)Br)c1I
Reaction #219172
N,N-Bis-[2-(2-bromopropionylamino)ethyl)-5-[(2-bromopropionyl)methylamino]-2,4,6-triiodoisophthalic acid amide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CC(Br)C(=O)NCCN(CCNC(=O)C(C)Br)C(=O)c1c(I)c(NC(=O)C(C)Br)c(I)c(C(=O)O)c1I
Reaction #219174
N,N-Bis-[2-(2-bromopropionylamino)ethyl)-5-[(2-bromopropionyl)amino]-2,4,6-triiodoisophthalic acid amide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CC(Br)C(=O)CNc1c(I)c(C(=O)O)c(I)c(C(=O)N(CCNC(=O)CNC(=O)C(C)Br)CCNC(=O)CNC(=O)C(C)Br)c1I
Reaction #219176
N,N-Bis-[2-(2-bromopropionylaminoacetylamino)ethyl)-5-[(2-bromopropionyl)methylamino]-2,4,6-triiodoisophthalic acid amide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CC(C)COC(=O)C(C)Br
Reaction #220490
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CC(Br)C(=O)c1ccc(Cl)cc1
Reaction #221301
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(Br)C(=O)c1ccc2sc(=O)[nH]c2c1
Reaction #238677
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
الصفحة 1التالي