An 136 Reaktionen beteiligt

C#CCCl

C#CCN1CCCCC1
Reaction #6885
1-(2-propynyl)piperidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C#CCOc1cccnc1Cl
Reaction #55315
2-chloro-3-(2-propynyloxy)pyridine
Ausbeute 52.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
C#CCOCc1cccnc1
Reaction #55318
3-(2-propynyloxymethyl)pyridine
Ausbeute 45.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CC#COc1ccncc1
Reaction #55319
4-(propynyloxy)pyridine
Ausbeute 3.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
C#CCSc1ccncc1
Reaction #55320
4-(2-propynylthio)pyridine
Ausbeute 40.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
Reaction #62732
needles
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
C#CCOc1cc(C(=O)OC)cc(OC)c1OC
Reaction #62738
methyl 3,4-dimethoxy-5-(2-propynyloxy)benzoate
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
C#CCOc1cc(C(C)C)c(Oc2cnc(N)nc2N)cc1I
Reaction #66666
5-(5-iodo-2-isopropyl-4-prop-2-ynyloxy-phenoxy)-pyrimidine-2,4-diamine
Ausbeute 71.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
C#CCOc1ccc(-n2cnnn2)nc1
Reaction #167822
5-(Prop-2-ynyloxy)-2-(1H-tetrazol-1-yl)pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
C#CCOc1cccnc1C
Reaction #167843
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
C#CCOc1cc(C(C)C)c(Oc2cnc(N)nc2N)cc1I
Reaction #168986
5-(5-iodo-2-isopropyl-4-prop-2-ynyloxy-phenoxy)-pyrimidine-2,4-diamine
Ausbeute 71.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
C#CCN1CCC(NS(=O)(=O)c2ccc(OCc3cc(C)nc4ccccc34)cc2)C(C)(C(=O)NOC(C)(C)C)C1
Reaction #178435
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C#CCC(C#N)(c1ccccc1)c1ccccc1
Reaction #201585
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C#CCOc1ccc(CCNC(=O)C(=COC(F)F)c2ccc(C)cc2)cc1OC
Reaction #228727
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
C#CCSc1cc(N)c(F)cc1Cl
Reaction #232444
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
C#CCNc1c(C)cccc1C
Reaction #274368
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
C#CCON=CC(C)=CC1C(C(=O)OC(C)(C)C)C1(C)C
Reaction #276968
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cl
Reaction #284326
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
C#CCOc1cc(Cc2cnc(N)nc2N)cc(OC)c1OC
Reaction #287903
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
C#CCN1C(=O)COc2ccc(N)cc21
Reaction #322768
6-amino-4-(2-propynyl)-2H-1,4-benzoxazin-3(4H)-one
Ausbeute 58.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_02
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