Hydrogen Bromide → HCID 16036676, compound

Participants

Reaction Steps

7-(2-Aminoethyl)-4-hydroxy-1,3-benzothiazol-2(3H)-one hydrochloride (176 mg) was dissolved in NMP (2 ml) to give a clear, yellow solution. Sodium hydroxide (27 mg) was dissolved in methanol (0.6 ml), and added in one portion to the yellow solution which turned bright orange. N-[2-(diethylamino)ethyl]-3-[2-(2-naphthyl)ethoxy]-N-(2-oxoethyl)propanamide (Example 32d) (458 mg) was dissolved in DCM (1 ml) and added drop-wise. The mixture was allowed to stir for 1 hour. Sodium triacetoxyborohydride (303 mg) was added portion-wise, and mixture stirred for 45 mins. Water (10 ml) was added followed by DCM, and the layers separated. The aqueous layer was extracted with DCM (×3). The remaining aqueous layer was found to contain desired material, so this was mixed with ethanol, then evaporated to dryness re-dissolved in methanol water mix, and loaded onto a pre-washed SCX cartridge. The cartridge was washed with 1:1 methanol:water, then methanol, then eluted with 0.07N methanolic ammonia to give a yellow film (178 mg). This was dissolved in ethanol, aqueous HBr (100 ul) added and the solution left to stand for 30 mins. The solvents were removed in vacuo to give a yellow solid, which was azeotroped with ethanol (×3). Ethanol was added and mixture sonicated to give a pale yellow suspension. Solid collected by filtration, and washed with ethanol to give the title compound (141 mg).

Provenance & Evidence