N-ethylethanamine

CCN(CC)c1ccc(C#N)cc1
Reaction #545
収率 39.2%750 AstraZeneca ELN dataset
CCN(CC)Cc1ccc([C@H]2CC[C@H](OC(C)=O)CC2)cc1
Reaction #1755
trans-O-Acetyl-4-(4-diethylaminomethylphenyl)-cyclohexanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1ccc(C#CCO)cc1
Reaction #1826
pale yellow solid
収率 83.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCN(CC)C(=O)CC(C)=O
Reaction #2937
title compound
収率 65.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCN(CC)CCC1CN(C)C(=S)c2cccnc2O1
Reaction #4927
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CCN(CC)CCC1CN(C)C(=O)c2cc(Cl)cnc2O1.O=C(O)C(=O)O
Reaction #4958
white crystals
収率 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=C1C(c2ccccc2)=C(c2ccccc2)CCC1c1ccccc1
Reaction #5147
2,3,6-triphenylcyclohexenone
収率 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C(O)CCC#Cc1ccccc1
Reaction #6818
5-phenylpent-4-ynoic acid
収率 28.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1ccccc1C#CCN1CCCCC1
Reaction #6884
oil
収率 62.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC1CCN(CC#Cc2cccc(F)c2)CC1
Reaction #6886
oil
収率 56.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
—
Reaction #7107
solid
収率 88.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)C(Cc1ccc(Oc2ccc(CC3SC(=O)NC3=O)cc2)cc1)NC(=O)C(N)Cc1c[nH]cn1.Cl.Cl
Reaction #7443
title compound
収率 163.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCN(CC)Cc1cc(-c2ccc(C)cc2)nn(CC(C)C)c1=O
Reaction #8040
title compound
収率 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
—
Reaction #8055
oil
収率 94.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCN(CC)Cc1cc(-c2ccc(F)cc2F)nn(CC(C)C)c1=O
Reaction #8069
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C=C(Cc1ccccc1)C(=O)O
Reaction #8402
2-methylene-3-phenylpropanoic acid
収率 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCC#Cc1ccccn1
Reaction #9274
title compound
収率 84.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCC#Cc1cc(OC)ccn1
Reaction #9282
2-(1-butynyl)-4-methoxypyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
—
Reaction #9421
solid
収率 88.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C=C(Cc1ccccc1)C(=O)O
Reaction #9878
compound 17
収率 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
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