Rhodamine dyes and conjugates
The present invention relates generally to novel rhodamine dyes which upon conjugation with another molecule form single isomeric conjugation products. These novel rhodamine dyes contain only one single functional group on the rhodomine molecule for conjugation so that their conjugation products are single isomeric conjugation products.
1. A compound comprising a rhodamine dye or a salt thereof having the general structure of
having a single functional group wherein the R1, R2, R3, R4 and R5 groups are independently selected as follows:
R5 is independently H
R4 is independently H or
R3 is independently H,
R2 is independently H or
and R1 is H.
2. The compound of claim 1 , wherein the salt is a pharmaceutically acceptable salt.
3. The compound of claim 2 , wherein the salt is selected from the group consisting of trifluoroacetate, chloride, hydrochloride, hydrobromide, hydroiodide, nitrate, sulfate, bisulfate, phosphate, acid phosphate, isonicotinate, acetate, lactate, salicylate, citrate, tartrate, pantothenate, bitartrate, ascorbate, succinate, maleate, gentisinate, fumarate, gluconate, glucuronate, saccharate, fortmate, benzoate, glutamate, methanesulfonate, ethanesulfonate, benzenesulfonate and p-toluenesulfonate.
4. The compound of claim 3 , wherein the salt is chlooride.
5. A method of making the compound of claim 1 , wherein R1, R3, and R5 are H, R2 is H or
and R4 is H or
the method comprising the steps of:
mixing 8-hydroxyjulolidine and 3-formyl benzoic acid in aqueous H 2 SO 4 .
6. A method of making the compound of claim 1 , wherein R1, R2, R4 and R5 are H and R3 is
the method comprising the steps of:
mixing 8-hydroxyjulolidine and 4-bromobenzaldehyde in aqueous H 2 SO 4 .
7. A method of making the compound of claim 1 , wherein R1, R2, R4 and R5 are H and R3 is
the method comprising the steps of:
preparing a reaction mixture comprising the compound of claim 1 wherein R1, R2, R4 and R5 are H and R3 is
and tert-butyl N-{[4-(dihydroxyboranyl)phenyl]methyl}carbamate in an aqueous solution of ethanol and K 2 CO 3 ;
degassing said reaction mixture; and
adding [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II).
8. A method of using the compound of claim 1 , wherein R1, R3, and R5 are H, R2 is H or
and R4 is H or
for making a rhodamine dye or a salt thereof having the general structure of
wherein R1, R3, and R5 are H, R2 is H or
and R4 is H or
wherein the R6 and/or R7 form a spacer which contains a single functional group, said method comprising the steps of:
dissolving said compound of claim 1 in DMF-CH 3 CN to form a solution;
preparing a reaction mixture by adding triethylamine and 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphorinane-2,4,6-trioxide in ethyl acetate to the solution; and
adding the reaction mixture to 1,2-diaminoethane, 1,3-diaminopropane, 1,6-diaminohexane, [4-(aminomethyl)phenyl]methanamine, piperidin-4-one or 2,2-dimethoxyethan-1-amine.
9. A method of using the compound of claim 1 , wherein R1, R2, R4 and R5 are H and R3 is
for making a rhodamine dye or a salt thereof having the general structure of
wherein R1, R2, R4 and R5 are H and R3 is
said method comprising the steps of:
dissolving said compound of claim 1 and 5-methyl-2-(4,4,5,5-tetramethyl)-1,3,2-dioxaborolan-2-yl)-phenylamine or 4-ethanone phenyl boronic acid in ethanol to form a solution;
preparing a reaction mixture by adding K 2 CO 3 and [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II)DCM to the solution; and
heating.
10. A method of using the compound of claim 1 , wherein R1, R2, R4 and R5 are H and R3 is
for making a rhodamine dye or a salt thereof having the general structure of
wherein R1, R2, R4 and R5 are H and R3 is
said method comprising the steps of:
dissolving said compound of claim 1 in DCM/TFA.