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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1670801Generated: October 30, 2026

Ammonium Bicarbonate → 5-[(R)-2-(2-{4-[4-(2-amino-2-methyl-propoxy)-phenylamino]-phenyl}-ethylamino)-1-hydroxy-ethyl]-8-hydroxy-1H-quinolin-2-one

https://huagongshe.com/reaction/1670801

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium BicarbonateHCID 14013—
ReactantTrifluoroacetateHCID 84468—
Reactant5-[(R)-2-(2-{4-[4-(2-amino-2-methyl-propoxy)-phenylamino]-phenyl}-ethylamino)-1-hydroxy-ethyl]-8-hydroxy-1H-quinolin-2-one trifluoroacetateHCID 86599721—
SolventEthanolHCID 702—
Product5-[(R)-2-(2-{4-[4-(2-amino-2-methyl-propoxy)-phenylamino]-phenyl}-ethylamino)-1-hydroxy-ethyl]-8-hydroxy-1H-quinolin-2-oneHCID 1116936580%

Reaction Steps

Aqueous ammonium bicarbonate (10%) solution (50 mL) was added in one portion to a solution of the product of Example 1, 5-[(R)-2-(2-{4-[4-(2-amino-2-methyl-propoxy)-phenylamino]-phenyl}-ethylamino)-1-hydroxy-ethyl]-8-hydroxy-1H-quinolin-2-one trifluoroacetate, (1.80 g, 2.1 mmol) in ethanol (6 mL). The solution was stirred at room temperature for 1 h. The resultant solid was filtered and dried under reduced pressure to afford the title compound (0.84 g, 1.67 mmol, 80%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07994165B2
Source datasetuspto-grants-2011_08
ORD IDord-f3de64ba23ec4ee58b6e32ae33097275
Source noteuspto-grants-2011_08