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763536

CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)[C@H]1CCCN1CCc1ccncc1.Cl
Reaction #11578
titled compound
Ausbeute 47.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C1Cn2c(=O)ccc3ncc(F)c1c32
Reaction #43397
solid
Ausbeute 36.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(CCl)c1c(F)cnc2cc(F)c(OC)nc12
Reaction #43413
8-[1-(Chloromethyl)ethenyl]-3,7-difluoro-2-(methyloxy)-1,5-naphthyridine
DOI: 10.6084/m9.figshare.5104873.v1
C=C1Cn2c(=O)c(F)cc3ncc(F)c1c32
Reaction #43414
3,8-Difluoro-4-methylidene-4,5-dihydro-7H-pyrrolo[3,2,1-de]-1,5-naphthyridin-7-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ncc(-c2ccnc3c2ccn3COCC[Si](C)(C)C)[nH]1
Reaction #69160
4-(2-tert-butyl-1H-imidazol-5-yl)-1-[2-(trimethylsilyl)ethoxy]methyl-1H-pyrrolo[2,3-b]pyridine
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1
C[Si](C)(C)CCOCn1ccc2c(C(=O)CCl)ccnc21
Reaction #69163
2-chloro-1-(1-[2-(trimethylsilyl)-ethoxy]methyl-1H-pyrrolo[2,3-b]pyridin-4-yl)ethanone
Ausbeute 35.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ncc(-c2ccnc3c2ccn3COCC[Si](C)(C)C)[nH]1
Reaction #73193
4-(2-tert-butyl-1H-imidazol-5-yl)-1-[2-(trimethylsilyl)ethoxy]methyl-1H-pyrrolo[2,3-b]pyridine
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1
C[Si](C)(C)CCOCn1ccc2c(C(=O)CCl)ccnc21
Reaction #73196
2-chloro-1-(1-[2-(trimethylsilyl)-ethoxy]methyl-1H-pyrrolo[2,3-b]pyridin-4-yl)ethanone
Ausbeute 35.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #172839
solid
Ausbeute 2.9%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)C1CCCN1CCc1ccncc1
Reaction #195770
DOI: 10.1039/C8SC04228D
Cn1c(=O)cc(CCN2CCN(c3nccc4sccc34)CC2)c2cc(F)ccc21
Reaction #222051
DOI: 10.1039/C8SC04228D
C=C(CCl)c1cc(Cl)nc(Cl)c1
Reaction #296022
DOI: 10.1039/C8SC04228D
CC(=O)OCC1=C(C(=O)OC(C)(C)C)N2C(=O)[C@@H](NC(=O)Cc3ccncc3)[C@H]2SC1
Reaction #345833
ester
DOI: 10.6084/m9.figshare.5104873.v1
C[Si](C)(C)CCOCn1ccc2c(C(=O)CCl)ccnc21
Reaction #390197
DOI: 10.1039/C8SC04228D
CC(O)(CCl)c1ccncc1
Reaction #398653
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCN(CCc2ccnc(C#N)c2)CC1
Reaction #400161
DOI: 10.1039/C8SC04228D
Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)Cc5ccncc5)nc4)c3Cl)c2n1
Reaction #452752
8-[2,6-dichloro-3-[N-methyl-N-[(E)-3-[6-(4-pyridylacetamido)pyridin-3-yl]acryloylglycyl]amino]-benzyloxy]-2-methyl-4-(2-pyridylmethoxy)quinoline
Ausbeute 9.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(OC)c(Sc2nc3c(N)ncnc3n2CCc2ccncc2)c1
Reaction #532250
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(CCc2ccnc(C#N)c2)CC1
Reaction #583801
1-Boc-4-[2-(2-cyanopyridin-4-yl)ethyl]piperazine
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(CCc2ccnc(C#N)c2)CC1
Reaction #673539
1-Boc-4-[2-(2-cyanopyridin-4-yl)ethyl]piperazine
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
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