Asymmetric benzoxanthene dyes
View Patent ↗A class of asymmetric monobenzoxanthene compounds useful as fluorescent dyes are disclosed having the structure wherein Y 1 and Y 2 are individually hydroxyl, amino, imminium, or oxygen, R 1 –R 8 are hydrogen, fluorine, chlorine, alkyl, alkene, alkyne, sulfonate, amino, amido, nitrile, alkoxy, linking group, and combinations thereof, and R 9 is acetylene, alkane, alkene, cyano, substituted phenyl, and combinations thereof. The invention further includes novel intermediate compounds useful for the synthesis of asymmetric benzoxanthene compounds having the general structure where substituents R 3 –R 7 correspond to like-referenced substituents in the structure of described above, and Y 2 is hydroxyl or amine. In another aspect, the invention includes methods for synthesizing the above dye compounds and intermediates. In yet another aspect, the present invention includes reagents labeled with the asymmetric benzoxanthene dye compounds, including deoxynucleotides, dideoxynucleotides, phosphoramidites, and polynucleotides. In an additional aspect, the invention includes methods utilizing such dye compounds and reagents including dideoxy polynucleotide sequencing and fragment analysis methods.
1. A phosphoramidite compound having the formula:
wherein:
B 1 is a phosphite ester protecting group;
B 2 and B 3 , taken separately, are selected from lower alkyl, lower alkene, aryl and cycloalkyl, containing up to 10 carbon atoms;
B 5 is selected from triphenylmethyl radical and electron-donating-substituted triphenylmethyl radical;
B is a nucleobase;
D comprises a dye of the formula:
wherein:
Y 1 and Y 2 taken separately are selected from the group consisting of hydroxyl, oxygen, imminium, and amine;
R 1 –R 8 taken separately are selected from the group consisting of hydrogen, fluorine, chlorine, lower alkyl, lower alkene, lower alkyne, sulfonate, sulfone, amino, imminium, amido, nitrile, lower alkoxy, linking group, and combinations thereof; and
R 9 is selected from the group consisting of acetylene, lower alkyl, lower alkene, cyano, phenyl, substituted phenyl, heterocyclic aromatic, and substituted phenyl having the structure:
wherein:
X 1 –X 5 taken separately are hydrogen, chlorine, fluorine, lower alkyl, carboxylic acid, sulfonic acid, —CH 2 OH, or linking group;
wherein when B is purine or 7-deazapurine, the sugar moiety is attached at the N 9 -position of the purine or 7-deazapurine, and when B is pyrimidine, the sugar moiety is attached at the N 1 -position of the pyrimidine;
wherein B and D are linked through a linkage attached to D at one of positions R 1 –R 9 ; and
wherein if B is a purine, the linkage is attached to the 8-position of the purine, if B is 7-deazapurine, the linkage is attached to the 7-position of the 7-deazapurine, and if B is pyrimidine, the linkage is attached to the 5-position of the pyrimidine.
2. The phosphoramidite compound of claim 1 wherein B 5 is an electron-donating-substituted triphenylmethyl radical.
3. The phosphoramidite compound of claim 2 wherein the electron-donating-substituted triphenylmethyl radical comprises at least one electron-donating substituent selected from amino, lower alkyl and lower alkoxy.
4. The phosphoramidite compound of claim 3 wherein the electron-donating substituent is lower alkoxy.
5. The phosphoramidite compound of claim 2 wherein the electron-donating-substituted triphenylmethyl radical is selected from 4,4′-dimethoxytrityl, monomethoxytrityl and tri(p-methoxyphenyl)methyl.
6. The phosphoramidite compound of claim 1 ,wherein
one of Y 1 and Y 2 is oxygen and the other is hydroxyl or protected phenolic hydroxyl,
R 9 is substituted phenyl wherein X 1 is carboxyl, X 2 and X 5 are chloro, and one of X 3 and X 4 is a linkage and the other is hydrogen, and either:
(a) R 1 and R 3 are fluoro, and R 2 and R 4 –R 8 are hydrogen,
(b) R 1 is chloro, R 3 is fluoro, and R 2 and R 4 –R 8 are hydrogen,
(c) R 1 is methoxy, R 2 is chloro, R 3 is fluoro, and R 4 –R 8 are hydrogen,
(d) R 3 is fluoro, and R 1 , R 2 and R 4 –R 8 are hydrogen,
(e) R 1 –R 8 are hydrogen,
(f) R 1 is chloro, and R 2 –R 8 are hydrogen, p 1 (g) R 1 is methoxy, R 2 is chloro, and R 3 –R 8 are hydrogen, or
(h) R 2 and R 3 are chloro, and R 1 and R 4 –R 8 are hydrogen.
7. The phosphoramidite compound of claim 6 wherein B 5 is an electron-donating-substituted triphenylmethyl radical.
8. The phosphoramidite compound of claim 7 wherein the electron-donating-substituted triphenylmethyl radical comprises at least one electron-donating substituent selected from amino, lower alkyl and lower alkoxy.
9. The phosphoramidite compound of claim 8 wherein the electron-donating substituent is lower alkoxy.
10. The phosphoramidite compound of claim 7 wherein the electron-donating-substituted triphenyhlmethyl radical is selected from 4,4′-dimethoxytrityl, monomethoxytrityl and tri(p-methoxyphenyl)methyl.
11. The phosphoramidite compound of claim 6 , wherein
R 1 and R 3 are fluoro, and R 2 and R 4 –R 8 are hydrogen.
12. The phosphoramidite compound of claim 6 , wherein
R 1 is chloro, R 3 is fluoro, and R 2 and R 4 –R 8 are hydrogen.
13. The phosphoramidite compound of claim 6 , wherein
R 1 is methoxy, R 2 is chloro, R 3 is fluoro, and R 4 –R 8 are hydrogen.
14. The phosphoramidite compound of claim 6 , wherein
R 3 is fluoro, and R 1 , R 2 and R 4 –R 8 are hydrogen.
15. The phosphoramidite compound of claim 6 , wherein
R 1 –R 8 are hydrogen.
16. The phosphoramidite compound of claim 6 , wherein
R 1 is chloro, and R 2 –R 8 are hydrogen.
17. The phosphoramidite compound of claim 6 , wherein
R 1 is methoxy, R 2 is chloro, and R 3 –R 8 are hydrogen.
18. The phosphoramidite compound of claim 6 , wherein
R 2 and R 3 are chloro, and R 1 and R 4 –R 8 are hydrogen.