The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Jan. 22, 2008

Filed:

Nov. 04, 2005
Applicants:

Marc A. Alvarez, Santa Fe, NM (US);

Rodolfo A. Martinez, Santa Fe, NM (US);

Clifford J. Unkefer, Los Alamos, NM (US);

Inventors:

Marc A. Alvarez, Santa Fe, NM (US);

Rodolfo A. Martinez, Santa Fe, NM (US);

Clifford J. Unkefer, Los Alamos, NM (US);

Assignee:

Los Alamos National Security, LLC, Los Alamos, NM (US);

Attorney:
Primary Examiner:
Assistant Examiner:
Int. Cl.
CPC ...
C07C 69/74 (2006.01); C07C 321/00 (2006.01); A61K 51/00 (2006.01);
U.S. Cl.
CPC ...
Abstract

The present invention is directed to labeled compounds of the formulae wherein R, R, R, Rand Rare each independently selected from the group consisting of hydrogen, a C-Clower alkyl, a halogen, and an amino group selected from the group consisting of NH, NHR and NRR' where R and R′ are each independently selected from the group consisting of a C-Clower alkyl, an aryl, and an alkoxy group, and X is selected from the group consisting of hydrogen, a C-Clower alkyl group, and a fully-deuterated C-Clower alkyl group. The present invention is also directed to a process of preparing labeled compounds, e.g., process of preparing [C]methacrylic acid by reacting a (CHCHO—C(O)—CH)— aryl sulfone precursor withCHI to form a (CHCHO—C(O)—C(CH))— aryl sulfone intermediate, and, reacting the (CHCHO—C(O)—C(CH))— aryl sulfone intermediate with sodium hydroxide, followed by acid to form [C]methacrylic acid. The present invention is further directed to a process of preparing [H]methyl methacrylate by reacting a (HOOC—C(CH)— aryl sulfinyl intermediate with CDI to form a (HCOOC—C(CH))— aryl sulfinyl intermediate, and heating the(HCOOC—C(CH))— aryl sulfinyl intermediate at temperatures and for time sufficient to form [H]methyl methacrylate.


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