Theodore A Adams

US Patent:

51867702, Feb 16, 1993

Filed:

Jun 29, 1984

Appl. No.:

6/626501

Inventors:

Theodore C. Adams - Beltsville MD
Horst G. Adolph - Silver Spring MD

Assignee:

The United States of America as represented by the Secretary of the Navy - Washington DC

International Classification:

C07C11100
C06B 2534

US Classification:

149 92

Abstract:

Bis(2-nitro-2-azapropyl) ether which is prepared by reacting one mole 1-hydroxy-2-nitro-2-azapropane with one mole of 2-nitro-2-azapropyl trifluoroacetate or 2-nitro-2-azapropyl acetate.

US Patent:

45672962, Jan 28, 1986

Filed:

Jun 29, 1984

Appl. No.:

6/626510

Inventors:

Theodore C. Adams - Beltsville MD
Horst G. Adolph - Silver Spring MD

Assignee:

The United States of America as represented by the Secretary of the Navy - Washington DC

International Classification:

C07C11100
C07C 6963
C06B 2534

US Classification:

564111

Abstract:

1-Fluoro-1,1,5-trinitro-3-oxa-5-azahexane which is prepared by reacting one mole of 2-fluoro-2,2-dinitroethanol with one mole of an acetate of the formula ##STR1## wherein R is --CF. sub. 3 or CH. sub. 3.

US Patent:

48777790, Oct 31, 1989

Filed:

May 17, 1988

Appl. No.:

7/194903

Inventors:

Waclaw J. Rzeszotarski - Millersville MD
John P. Carter - Baltimore MD
Theodore C. Adams - Perry Hall MD
Andrea C. Dupont - Lutherville MD
Carl Kaiser - Millersville MD

Assignee:

Marion Laboratories, Inc. - Kansas City MO

International Classification:

A61K 31385
A61K 31535
C07D40512
C07D33908

US Classification:

514 63

Abstract:

Novel compounds and their salts are disclosed having the Formulas: ##STR1## wherein: R. sub. 1 is hydrogen, phenyl, 9H-fluoren-9-yl, 10,11-dihydro-5H-dibenzo [a,d]cyclohepten-5-yl, 5H-dibenzo[a,d]cyclohepten-5-yl, 1,2,3,4-tetrahydro-1-naphthyl, 9H-xanthen-9-yl, 9H-thioxanthen-9-yl, 2-chloro-9H-thioxanthen-9-yl, 4H-chromanyl, diphenylmethyl, phenylcycloalkylmethyl wherein the bridgehead methylene may optionally be substituted with a hydroxy group and any of the phenyl or benzo-fused rings may be substituted with one or more R. sub. 5 groups wherein R. sub. 5 is selected from halogen, trifluoromethyl, lower alkyl, hydroxy or lower alkoxy groups; and R. sub. 2 and R. sub. 3, which may be the same or different, are hydrogen, lower alkyl, phenylalkyl (C. sub. 1 -C. sub. 5), wherein the phenyl ring may be substituted with one or more R. sub. 5 groups or NR. sub. 2 R. sub.