An 156 Reaktionen beteiligt

1379156

C[C@@H]1CCCN(C(=O)c2ccccc2-c2ncccn2)[C@@H]1CNc1ccc(C(F)(F)F)cn1
Reaction #89527
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C(O)c1ccccc1Nc1ccnn1C1CCCC1
Reaction #197411
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(O)c1ccccc1Sc1cccc2ccccc12
Reaction #200612
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=CCCCCC(O)COc1ccc(F)cc1
Reaction #200640
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(Cl)c1ccccc1I
Reaction #226423
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1cc(Nc2ccccc2C(=O)O)n(C)n1
Reaction #242300
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)C(NC(=O)c1ccccc1I)c1ccccc1I
Reaction #246515
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1cc(Nc2ccccc2C(=O)O)n(-c2ccccn2)n1
Reaction #263282
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(Cl)c1ccccc1I
Reaction #276908
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCn1nc(C)cc1Nc1ccccc1C(=O)O
Reaction #281852
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1ccccc1Sc1ccccc1C(=O)O
Reaction #286360
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(Cl)c1ccccc1I
Reaction #323561
ortho-iodobenzoic acid chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_02
O=Cc1ccc(N2CCNCC2CCOCCO)cc1I
Reaction #338576
4-[2-(2-hydroxy-ethoxy)ethyl-piperazin-1-yl}-(2-iodophenyl)-methanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
COc1ccccc1Sc1ccccc1C(=O)O
Reaction #343107
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_10
O=C(O)c1ccccc1Nc1ccnn1C1CCCC1
Reaction #396115
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCCCC(=O)CCCC
Reaction #397523
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C(c1ccccc1I)c1nc(CCN2CCOCC2)n2ccccc12
Reaction #401726
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C(O)c1ccccc1Oc1ccc(F)cc1
Reaction #408651
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C(Nc1ccc([N+](=O)[O-])cc1O)Nc1ccccc1I
Reaction #410250
desired compound
Ausbeute 13.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
O=C(Cl)c1ccccc1I
Reaction #443598
2-iodobenzoyl chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_11
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