IP Library Granted Patent US 9,062,205
Granted Patent B2
US 9,062,205 · App. 13/482,528 · Granted Jun 23, 2015

Alkyl amine compounds for fluorescent labeling

Inventors: Michael W. Reed (Lake Forest Park, WA); Robert O. Dempcy (Kirkland, WA)
Assignee: Blood Cell Storage, Inc.
C09B11/24C09B11/245C09B62/4401C07F9/6561C07H21/00C07C233/05C07D493/10
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,062,205
App. No.
13/482,528
Granted
Jun 23, 2015
Kind
B2
Abstract

Alkyl amine dyes, oligonucleotide probes prepared from the alkyl amine dyes, phosphoramidites and solid supports prepared from the alkyl amine dyes, and methods of labeling biological agents using the alkyl amine dyes.

Claims (27)

1. A compound having the formula (III) or (IV):

their salts, active esters, acid/base forms, and tautomers, wherein

A 1 and A 2 are independently selected from hydroxy, amino, mono- and dialkyl amino, protected hydroxy, protected amino, protected mono- and dialkyl amino, or when A 1 or A 2 is amino, mono- and dialkyl amino, A 1 and/or A 2 taken together with R 2 and/or R 4 (for A 1 ) or with R 1 (for A 2 ) and the atoms to which they are attached form a 5- or 6-membered nitrogen-containing ring;

R 1 ′, R 1 , R 2 , R 3 , R 4 , and R 5 are each independently selected from the group consisting of hydrogen, halogen, cyano, trifluoromethyl, (C 1 -C 8 )alkyl, (C 1 -C 8 )alkylthio and (C 1 -C 8 )alkoxy, aryl, and heteroaryl;

R 6 is halogen;

X 1 , X 2 , X 3 , and X 4 are each independently selected from the group consisting of hydrogen, halogen, cyano, trifluoromethyl, (C 1 -C 8 )alkyl, (C 1 -C 8 )alkoxy, (C 1 -C 8 )alkylthio, (C 2 -C 8 )alkenyl, (C 2 -C 8 )alkynyl, aryl, aryl(C 1 -C 4 )alkyl, heteroaryl, SO 3 H and CO 2 H,

wherein the alkyl portions of any of R 1 ′ and R 1 -R 6 and X 1 -X 4 are optionally substituted with halogen, carboxy, sulfo, amino, mono- or dialkylamino, alkoxy, cyano, haloacetyl or hydroxy, and the alkyl portions of the substituents have from 1 to 6 carbon atoms;

and wherein the aryl or heteroaryl portions of any of R 1 ′ and R 1 -R 6 and X 1 -X 4 are optionally substituted with from one to four substituents selected from the group consisting of halogen, cyano, carboxy, sulfo, hydroxy, amino, mono- or di(C 1 -C 6 )alkylamino, (C 1 -C 6 )alkyl, (C 1 -C 6 )alkylthio and (C 1 -C 6 )alkoxy;

wherein L 1 has a length not exceeding the length of a normal alkyl chain of 25 carbons and comprises from one to about 50 atoms,

wherein L 2 has a length not exceeding the length of a normal alkyl chain of 25 carbons and comprises from one to about 50 atoms, and

wherein FG is a functional group reactive toward and capable of covalently coupling the fluorescent dye compound to a suitably reactive material.

2. A compound having the formula:

its salts, active esters, acid/base forms, and tautomers.

3. A compound having the formula (III) or (IV):

their salts, active esters, acid/base forms, and tautomers, wherein

A 1 and A 2 are independently selected from hydroxy, amino, mono- and dialkyl amino, protected hydroxy, protected amino, protected mono- and dialkyl amino, or when A 1 or A 2 is amino, mono- and dialkyl amino, A 1 and/or A 2 taken together with R 2 and/or R 4 (for A 1 ) or with R 1 (for A 2 ) and the atoms to which they are attached form a 5- or 6-membered nitrogen-containing ring;

R 1 ′, R 1 , R 2 , R 3 , and R 5 are each independently selected from the group consisting of hydrogen, halogen, cyano, trifluoromethyl, (C 1 -C 8 )alkyl, (C 1 -C 8 )alkylthio and (C 1 -C 8 )alkoxy, aryl, and heteroaryl;

R 4 and R 6 are halogen;

X 1 , X 2 , X 3 , and X 4 are each independently selected from the group consisting of hydrogen, halogen, cyano, trifluoromethyl, (C 1 -C 8 )alkyl, (C 1 -C 8 )alkoxy, (C 1 -C 8 )alkylthio, (C 2 -C 8 )alkenyl, (C 2 -C 8 )alkynyl, aryl, aryl(C 1 -C 4 )alkyl, heteroaryl, SO 3 H and CO 2 H,

wherein the alkyl portions of any of R 1 ′ and R 1 -R 6 and X 1 -X 4 are optionally substituted with halogen, carboxy, sulfo, amino, mono- or dialkylamino, alkoxy, cyano, haloacetyl or hydroxy, and the alkyl portions of the substituents have from 1 to 6 carbon atoms; and wherein the aryl or heteroaryl portions of any of R 1 ′ and R 1 -R 6 and X 1 -X 4 are optionally substituted with from one to four substituents selected from the group consisting of halogen, cyano, carboxy, sulfo, hydroxy, amino, mono- or di(C 1 -C 6 )alkylamino, (C 1 -C 6 )alkyl, (C 1 -C 6 )alkylthio and (C 1 -C 6 )alkoxy;

wherein L 1 has a length not exceeding the length of a normal alkyl chain of 25 carbons and comprises from one to about 50 atoms,

wherein L 2 has a length not exceeding the length of a normal alkyl chain of 25 carbons and comprises from one to about 50 atoms, and

wherein FG is a functional group reactive toward and capable of covalently coupling the fluorescent dye compound to a suitably reactive material.

4. The compound of claim 1 , wherein R 6 is chloro.

5. The compound of claim 3 , wherein R 4 is chloro.

6. The compound of claim 3 , wherein R 6 is chloro.

7. The compound of claim 3 , wherein R 4 and R 6 are chloro.

Assignments (3)
SECURITY INTEREST Recorded May 30, 2014
From: BLOOD CELL STORAGE, INC.
To: DOUGLAS A. BEVIS, IN HIS CAPACITY AS COLLATERAL AGENT
Reel/Frame 033062/0390 →
SECURITY INTEREST Recorded Mar 12, 2014
From: BLOOD CELL STORAGE, INC.
To: BEVIS, IN HIS CAPACITY AS COLLATERAL AGENT, DOUGLAS A.
Reel/Frame 032418/0372 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 4, 2012
From: REED, MICHAEL W.; DEMPCY, ROBERT O.
To: BLOOD CELL STORAGE, INC.
Reel/Frame 028892/0727 →
Continuity (3)
Provisional Application 61491107 · May 27, 2011
Provisional Application 61650304 · May 22, 2012
Related Publication 20120301880A1 · Nov 29, 2012