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6418

O=C(CCCBr)Nc1ccccc1Cc1ccccc1
Reaction #1051
2-benzyl-1-(4-bromobutyrylamino)benzene
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCCCCBr)Nc1ccccc1Cc1ccccc1
Reaction #1052
2-benzyl-1-(6-bromohexanoylamino)benzene
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCCBr)N1CC(c2ccc(Cl)cc2)Sc2ccccc21
Reaction #5923
4-(4-bromobutyryl)-2-(4-chlorophenyl)-3,4-dihyro-2H-1,4-benzothiazine
Ausbeute 93.2%DOI: 10.6084/m9.figshare.5104873.v1
CSc1cc(C)nc(SC)c1NC(=O)CCCBr
Reaction #51162
4-bromo-N-[2,4-bis(methylthio)-6-methyl-3-pyridyl]butanamide
Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCCBr)N1CCCC2CCCCC21
Reaction #67495
4-bromo-1-(octahydroquinolin-1-yl)butan-1-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCCBr)NCc1cc(Oc2ccc3c(ccn3C(=O)Nc3ccc(F)c(C(F)(F)F)c3)c2)ncn1
Reaction #73412
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #82906
Formula IX
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC(CC)CN(CC(CC)CCCC)C(=O)CCBr
Reaction #89799
3-bromo-N,N-bis(2-ethylhexyl)propanamide
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)[C@@H]1CSC(c2ccccc2O)N1C(=O)CCBr
Reaction #96278
product
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCCBr)N1CCCC2CCCCC21
Reaction #155512
4-bromo-1-(octahydroquinolin-1-yl)butan-1-one
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)C(=O)CCBr
Reaction #157629
3-Bromo-N,N-diethylpropanamide
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(Cl)ccc1SCCC(=O)N1CCCC1
Reaction #157632
title compound
Ausbeute 50.9%DOI: 10.6084/m9.figshare.5104873.v1
C=CC(=O)N1CCC(Nc2ncc3c(n2)-c2c(c(C(=O)Nc4c(CC)cccc4CC)nn2C)CC3)CC1
Reaction #169141
8-[(1-Acryloylpiperidin-4-yl)amino]-N-(2,6-diethylphenyl)-1-methyl-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxamide
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCCBr)Nc1cccc(I)c1
Reaction #169226
title compound
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCN1c1cccc(-c2n[nH]c(C3CCCCN3C(=O)COc3ccccc3)n2)c1
Reaction #176129
DOI: 10.1039/C8SC04228D
CC(C)(C)c1ccc(C(=O)NC(=S)Nc2ccc(NC(=O)CCCCCCCBr)cc2)cc1
Reaction #181884
DOI: 10.1039/C8SC04228D
O=C(CCCCCCCBr)c1ccc(Cl)cc1
Reaction #182476
DOI: 10.1039/C8SC04228D
Cc1nc(NC(=O)CCCBr)sc1C(=O)NCc1ccc(F)cc1
Reaction #183038
DOI: 10.1039/C8SC04228D
O=C(Cl)CCCCCCCBr
Reaction #184377
DOI: 10.1039/C8SC04228D
O=C(Cl)CCCCCCCCCCBr
Reaction #188334
DOI: 10.1039/C8SC04228D
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