1-bromo-3-methoxypropane

COCCCN(N=C(C)C)C(=O)OC(C)(C)C
Reaction #41184
N′-isopropylidene-N-(3-methoxypropyl)-hydrazinecarboxylic acid tert-butyl ester
収率 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
—
Reaction #51280
Compound 1f
収率 73.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COCCCN[C@@H]1CCN(c2ccc(N3CCc4cc(OC[C@@H]5CCCO5)ccc4C3=O)cc2F)C1
Reaction #156690
2-{3-Fluoro-4-[(R)-3-(3-methoxy-propylamino)-pyrrolidin-1-yl]-phenyl}-6-[(S)-1-(tetrahydro-furan-2-yl)methoxy]-3,4-dihydro-2H-isoquinolin-1-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Br.COCCCn1ccsc1=N
Reaction #165579
title compound
収率 48.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Br.COCCCn1c(=N)sc2ccccc21
Reaction #165590
title compound
収率 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COCCCN(CCN1CCS(=O)(=O)CC1)S(=O)(=O)c1ccccc1[N+](=O)[O-]
Reaction #172747
title compound
収率 109.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COCCCSc1cnc(Nc2nc(C3COC4(CCCCC4)O3)ns2)c(Oc2cccnc2C)c1
Reaction #176269
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COCCCOc1ccc(C)c(Cn2ccc(NC(=O)c3c(F)cccc3F)n2)c1
Reaction #187559
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COCCCC1(O)CC2(CCCC2)c2ccccc21
Reaction #224049
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)C(C)=NNc1ccc(OCCCOC)cc1[N+](=O)[O-]
Reaction #272476
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COCCC[SiH](C(C)C)C(C)C
Reaction #272651
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COCCCNc1c(C(=O)OC)cccc1[N+](=O)[O-]
Reaction #276455
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COCCCOc1cc(C(=O)OC)ccc1C(C)(C)C
Reaction #287113
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COCCCOc1cc(C(C)=O)cc(C(C)(C)C)c1OC
Reaction #297685
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COCCCc1cc(C(OC)OC)c(Cl)cn1
Reaction #302054
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COCCCn1cnc2ccccc21
Reaction #302083
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Br.COCCCn1ccsc1=N
Reaction #342229
title compound
収率 48.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
Br.COCCCn1c(=N)sc2ccccc21
Reaction #342251
title compound
収率 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
[NH4+].[OH-]
Reaction #342320
NH4OH
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
COCCCOc1cc(C=O)ccc1OCc1ccccc1
Reaction #352093
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
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