tert-butyl 4-(4-formyl-1,3-thiazol-2-yl)piperidine-1-carboxylate

O=Cc1csc(C2CC[NH2+]CC2)n1.[Cl-]
Reaction #67009
4-(4-Formyl-1,3-thiazol-2-yl)piperidinium chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(C)(C)OC(=O)N1CCC(c2nc(C=NO)cs2)CC1
Reaction #157981
tert-Butyl 4-{4-[(hydroxyimino)methyl]-1,3-thiazol-2-yl}piperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
C=Cc1csc(C2CCN(C(=O)OC(C)(C)C)CC2)n1
Reaction #203228
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)N1CCC(c2nc(C3=NOC(c4ccccc4)C3)cs2)CC1
Reaction #325833
title compound
收率 43.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
Cl.O=Cc1csc(C2CCNCC2)n1
Reaction #325834
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
C=Cc1csc(C2CCN(C(=O)OC(C)(C)C)CC2)n1
Reaction #325838
title compound
收率 95.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC(C)(C)OC(=O)N1CCC(c2nc(C3=NOC(c4ccccc4)C3)cs2)CC1
Reaction #379473
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC(C)(C)OC(=O)N1CCC(c2nc(C=Cc3cccc4ccccc34)cs2)CC1
Reaction #401092
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC(C)(C)OC(=O)N1CCC(c2nc(/C=C/c3cccc4ccccc34)cs2)CC1
Reaction #637122
tert-Butyl 4-{4-[(E)-2-(naphthalen-1-yl)ethenyl]-1,3-thiazol-2-yl}piperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_05
CC(C)(C)OC(=O)N1CCC(c2nc(/C=C\c3cccc4ccccc34)cs2)CC1
Reaction #637123
tert-Butyl 4-{4-[(Z)-2-(naphthalen-1-yl)ethenyl]-1,3-thiazol-2-yl}piperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_05
CC(C/C=C\c1csc(C2CCN(C(=O)OC(C)(C)C)CC2)n1)c1ccccc1
Reaction #637124
tert-Butyl 4-{4-[(1Z)-4-phenylpent-1-en-1-yl]-1,3-thiazol-2-yl}piperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_05
C#Cc1csc(C2CCN(C(=O)OC(C)(C)C)CC2)n1
Reaction #637128
tert-Butyl 4-(4-ethynyl-1,3-thiazol-2-yl)piperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_05
CC(C)(C)OC(=O)N1CCC(c2nc(CNc3ccc(F)nc3)cs2)CC1
Reaction #773562
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CC(C)(C)OC(=O)N1CCC(c2nc(C=Cc3cccc4ccccc34)cs2)CC1
Reaction #910231
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
C#Cc1csc(C2CCN(C(=O)OC(C)(C)C)CC2)n1
Reaction #911279
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC(c2nc(CNc3ccc(F)nc3)cs2)CC1
Reaction #959117
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_03
[Cl-]
Reaction #1303692
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
CC(CC=Cc1csc(C2CCN(C(=O)OC(C)(C)C)CC2)n1)c1ccccc1
Reaction #1308535
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
CC(C)(C)OC(=O)N1CCC(c2nc(CNc3ccc(F)nc3)cs2)CC1
Reaction #1495545
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_12
CC(C)(C)OC(=O)N1CCC(c2nc(C=C(Br)Br)cs2)CC1
Reaction #1552619
tert-butyl 4-[4-(2,2-dibromovinyl)-1,3-thiazol-2-yl]piperidine-1-carboxylate
收率 97.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_04
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