Reaction #2146767

ord-189a52ba4aff4092ad6a3151f3bd5c85

Reaction equation

CN(C)C(=O)CN1CCC(Oc2cc3cc[nH]c(=O)c3cc2Cl)CC1
2-[4-(7-Chloro-1-oxo-1,2-dihydro-isoquinolin-6-yloxy)-piperidin-1-yl]-acetamide
CN(C)C(=O)CN1CCC(Oc2cc3cc[nH]c(=O)c3cc2Cl)CC1
2-[4-(7-Chloro-1-oxo-1,2-dihydro-isoquinolin-6-yloxy)-piperidin-1-yl]-N,N-dimethyl-acetamide
CCCN
propylamine
→
CCCNC(=O)CN1CCC(Oc2cc3cc[nH]c(=O)c3cc2Cl)CC1
title compound
CCCNC(=O)CN1CCC(Oc2cc3cc[nH]c(=O)c3cc2Cl)CC1
2-[4-(7-Chloro-1-oxo-1,2-dihydro-isoquinolin-6-yloxy)-piperidin-1-yl]-N-propyl-acetamide

Reactants

CN(C)C(=O)CN1CCC(Oc2cc3cc[nH]c(=O)c3cc2Cl)CC1
2-[4-(7-Chloro-1-oxo-1,2-dihydro-isoquinolin-6-yloxy)-piperidin-1-yl]-acetamide
CN(C)C(=O)CN1CCC(Oc2cc3cc[nH]c(=O)c3cc2Cl)CC1
2-[4-(7-Chloro-1-oxo-1,2-dihydro-isoquinolin-6-yloxy)-piperidin-1-yl]-N,N-dimethyl-acetamide
CCCN
propylamine

Reagents

None

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Procedure

The title compound was synthesized following the method described for 2-[4-(7-Chloro-1-oxo-1,2-dihydro-isoquinolin-6-yloxy)-piperidin-1-yl]-acetamide (43), using propylamine. Rt=0.98 min (Method B). Detected mass: 378.2 (M+H+).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08278294B2uspto-grants-2012_10