Abstract: The present invention is a novel process for the transformation of 17&agr;-hydroxy-6&agr;-methylpregn-4-ene-3,20-dione 17-acetate (I)
to 11&bgr;,17&agr;,21-trihydroxy-6&agr;-methylpregna-1,4-diene-3,20-dione 21-acetate (VI)
Type:
Grant
Filed:
June 14, 2002
Date of Patent:
December 7, 2004
Assignee:
Pharmacia and Upjohn Company
Inventors:
Bruce Allen Pearlman, Michael J. White, Ivan G. Gilbert
Abstract: The present invention is a container for an IV aqueous solution of a Gram-positive oxazolidinone agent, such as linezolid a the compound of formula:
which comprises having the container-solution contact surface material be a polyolefin.
Type:
Grant
Filed:
March 15, 2001
Date of Patent:
September 28, 2004
Assignee:
Pharmacia & Upjohn Company
Inventors:
Sandra M. Sims, Phil Bryan Bowman, Daniel C. Wade, Shri C. Valvani
Abstract: The present invention is a process for the conversion of bisnoralcohol to bisnoraldehyde (II), which is a known intermediate in the synthesis of progesterone.
Abstract: The present invention is a process, including intermediates, to produce (2S)-2-dipropylamino)-6-ethoxy-2,3-dihydro-1H-indene-5-carboxamide
which is a useful pharmaceutical agent.
Type:
Grant
Filed:
June 6, 2002
Date of Patent:
June 10, 2003
Assignee:
Pharmacia & Upjohn Company
Inventors:
Jiong Jack Chen, Arthur Glenn Romero, Styrbjorn Bystrom
Abstract: The present invention provides a compressed tablet of an antibacterial oxazolidinone agent which provides high drug load and excellent bioavailability.
Abstract: The present invention is a process to prepare on of a phenylisoserine ester of the formula (II)
&phgr;—CH(NH—CO—CH3)—CH(OH)—CO—O—R1
with reduced amount of diol by-product by the use of a compound of the formula R2—CO—NH2 where R2 is C1-C6 alkyl with the proviso that R2 is not tertiary.
Abstract: The present invention includes a number of novel intermediates such as the (S)-secondary alcohol of formula (VIIIA)
X2—CH2—C*H(OH)—CH2—NH—CO—RN (VIIIA)
and processes for production of pharmacologically useful oxazolidinones.
Abstract: The present invention are substituted 9-arylsulfone-1,2,3,4,5,6-hexahydroazepino[4,5-b]indoles (X) and unsubstituted 9-arylsulfone-1,2,3,4,5,6-hexahydroazepino[4,5-b]indoles (XI) such as the compound of EXAMPLE 13
which are useful in treating depression, obesity and other CNS disorders.
Type:
Grant
Filed:
July 11, 2000
Date of Patent:
October 22, 2002
Assignee:
Pharmacia & Upjohn Company
Inventors:
Eric Jon Jacobsen, Susan Korynne Hendges
Abstract: The present invention is a process, including intermediates, to produce (2S)-2-dipropylamino)-6-ethoxy-2,3-dihydro-1H-indene-5-carboxamide
which is a useful pharmaceutical agent.
Type:
Grant
Filed:
September 14, 2001
Date of Patent:
October 8, 2002
Assignee:
Pharmacia & Upjohn Company
Inventors:
Jiong Jack Chen, Arthur Glenn Romero, Styrbjorn Bystrom
Abstract: The present invention is a method of treating sexual disturbances in humans and inducing mating in non-human mammals using the compounds of formula (A)
in a dosage range where the sexually therapeutic amount is from about 0.2 thru 8 mg/person/dose and where the sexually mating amount is from about 0.003 thru 0.2 mg/kg/dose.
Type:
Grant
Filed:
December 17, 1999
Date of Patent:
September 24, 2002
Assignee:
Pharmacia & Upjohn Company
Inventors:
Martin Durham Meglasson, Robert B. McCall
Abstract: The present invention relates to two novel crystal forms of a known compound, 1-[5-Methanesulfonamidoindolyl-2-carbonyl]-4-[3-(1-methylethylamino)-2-pyridinyl] piperazine monomethanesulfonate salt, which are useful for treating humans who are HIV positive, which are identified by a powder X-ray diffraction spectrum known commonly as the “S” and “T” forms.
Abstract: The present invention includes a number of novel intermediates such as the (S)-secondary alcohol of formula (VIIIA)
X2—CH2—C*H(OH)—CH2—NH—CO—RN (VIIIA)
and processes for production of pharmacologically useful oxazolidinones.
Abstract: The process of the present invention transforms a steroidal ketone of formula (III)
to androst-4-en-17&bgr;-carboxylic acid (IV)
by reaction with K2SO5.KHSO4.K2SO4.
Abstract: The present invention includes a number of novel intermediates such as the (S)-secondary alcohol of formula (VIIIA)
X2—CH2—C*H(OH)—CH2—NH—CO—RN (VIIIA)
and processes for production of pharmacologically useful oxazolidinones.
Abstract: The present invention is an improved prosess to prepare (5R)-(methylamino)-5,6-dihydro-4H-imidazo[4,5,1-ij]quinolin-2(1H)-one the compound of formula (VII).
Abstract: The present invention involves a method of treating an ophthalmic infection in a useful warm blooded mammal who is in need of such treatment which comprises topical administration of an ophthalmologically effective amount of an OXAZOLIDINONE.
Abstract: The present invention includes processes to prepare commercially important taxols (X)
from substituted amino-3-phenyl (2R,3S) isoserinates (II). In addition processes to prepare the substituted amino-3-phenyl (2R,3S) isoserinates (II) as well as its precursor are set forth.
Abstract: The compound of the present invention (R)-3-hydroxy-3-(2-phenylethyl)-hexanoic acid
is an intermediate in the preparation of the anti-AIDS compound, [R-(R*,R*)]-N-[3-[1-5,6-dihydro-4-hydroxy-2-oxo-6-(2-phenylethyl)-6-propyl-2H-pyran-3-yl]propyl]phenyl]-5-(trifluoromethyl)-2-pyridinesulfonamide.
Type:
Grant
Filed:
February 28, 2000
Date of Patent:
July 24, 2001
Assignee:
Pharmacia & Upjohn Company
Inventors:
James R. Gage, Robert Charles Kelly, Bradley D. Hewitt
Abstract: The invention is a process for the preparation of cyclic-sulfur fluorine containing oxazolidinone antibacterial agents which utilizes the important tetrahydrothiopyran-o-fluorinated carbamate of formula (IV)