2-(7-methoxynaphthalen-1-yl)ethanamine;hydrochloride

Br.NCCc1cccc2ccc(O)cc12
Reaction #65565
2-(7-hydroxy-1-naphthyl)ethylamine hydrobromide
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
Br.NCCc1cccc2ccc(O)cc12
Reaction #80568
2-(7-hydroxy-l-naphthyl)ethylamine hydrobromide
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
COc1ccc2cccc(CCNC(C)=O)c2c1
Reaction #330818
agomelatine
Ausbeute 86.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
COc1ccc2cccc(CCNC(C)=O)c2c1
Reaction #330819
agomelatine
Ausbeute 86.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
COc1ccc2cccc(CCNC(C)=O)c2c1
Reaction #330820
agomelatine
Ausbeute 78.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
COc1ccc2cccc(CCNC(=O)CCCCl)c2c1
Reaction #570578
N-[2-(7-Methoxynaphth-1-Yl)Ethyl]-4-Chlorobutyramide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_07
COc1ccc2cccc(CCNC(=O)Cc3c[nH]cn3)c2c1
Reaction #570581
N-[2-(7-Methoxynaphth-1-Yl)Ethyl]-4-Imidazolylacetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_07
COc1ccc2cccc(CCNC(=O)CCCCl)c2c1
Reaction #1196221
N-[2-(7-METHOXYNAPHTH-1-YL)ETHYL]-4-CHLOROBUTYRAMIDE
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1994_06
COc1ccc2cccc(CCNC(=O)Cc3c[nH]cn3)c2c1
Reaction #1196224
N-[2-(7-METHOXYNAPHTH-1-YL)ETHYL]-4-IMIDAZOLYLACETAMIDE
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1994_06
COc1ccc2cccc(CCNC(C)=O)c2c1
Reaction #1384736
title product
Ausbeute 92.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_07
COc1ccc2cccc(CCNC(C)=O)c2c1
Reaction #1598349
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_07
COc1ccc2cccc(CCNC(=O)CCCCl)c2c1
Reaction #1701087
N-[2-(7-methoxynaphth-1-yl)ethyl]-4chlorobutyramide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_03
COc1ccc2cccc(CCNC(=O)Cc3c[nH]cn3)c2c1
Reaction #1701089
N-[2-(7-Methoxynaphth-1-yl)Ethyl]-4-Imidazolylacetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_03
COc1ccc2cccc(CCNC(C)=O)c2c1
Reaction #1869725
title product
Ausbeute 92.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_03
COc1ccc2cccc(CCNC(C)=O)c2c1
Reaction #1869729
title product
Ausbeute 92.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_03
COc1ccc2cccc(CCNC(C)=O)c2c1
Reaction #2072186
title product
Ausbeute 92.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_06