Synthèse de la diméthoxy‐6,7 ( para ‐chlorobenzyl)‐4 isoquinoléine, deutériée en position 3 ou marquée au  14 C sur le méthylène benzylique | Zendy

Bouvier P. | Zendy; Mourlevat F. | Zendy; Pichat L. | Zendy; Servin A. | Zendy; Viel C. | Zendy

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Synthèse de la diméthoxy‐6,7 ( para ‐chlorobenzyl)‐4 isoquinoléine, deutériée en position 3 ou marquée au 14 C sur le méthylène benzylique

Author(s) -

Bouvier P.,

Mourlevat F.,

Pichat L.,

Servin A.,

Viel C.

Publication year - 1987

Publication title -

journal of labelled compounds and radiopharmaceuticals

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.432

H-Index - 47

eISSN - 1099-1344

pISSN - 0362-4803

DOI - 10.1002/jlcr.2580240411

Subject(s) - chemistry , isoquinoline , medicinal chemistry , methylene , condensation reaction , stereochemistry , organic chemistry , catalysis

6,7‐dimethoxy‐4 ( para chlorobenzyl) (D‐3) isoquinoline : 6 and 6,7‐dimethoxy‐4 [ para chlorobenzyl (methylene 14 C)] isoquinoline: 11 were prepared respectively by the condensation of α‐deuterio‐veratrylaminoacetaldehyde diethylacetal : 4 with para chlorobenzaldehyde and the reaction of para chlorobenzaldehyde (carbonyl 14 C) : 9 with veratrylaminoacetaldehyde diethylacetal.

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