Dimethylamine → 1-(cyclohexyl)methyl-3-{4-[(dimethylamino)methyl]-5-ethyl-[1,3]-thiazol-2-yl}-7-methoxy-1H-indole, hydrochloride salt

Lithium borohydride (200 mg, 9.09 mmol) was added portionwise to a mixture of 2-(1-cyclohexylmethyl-7-methoxy-1H-indol-3-yl)-5-ethyl-thiazole-4-carboxylic acid ethyl ester (490 mg, 1.15 mmol) and tetrahydrofuran (5 ml) under ice-water cooling and the resulting mixture was stirred at 0° C. for 2 h. The reaction mixture was quenched with aqueous hydrochloric acid (2 M; 2 ml), and the aqueous layer extracted with dichloromethane (2×100 ml). The organic layers were combined, dried over magnesium sulfate, and concentrated in vacuo to yield the crude product. Silica gel column chromatography eluting with 66% ethyl acetate in heptane gave crude [2-(1-cyclohexylmethyl-7-methoxy-1H-indol-3-yl)-5-ethyl-thiazole-4-yl]-methanol (210 mg). This material was used in the next step without further purification. Methanesulfonylchloride (90 μl, 1.16 mmol) was added to a mixture of [2-(1-cyclohexylmethyl-7-methoxy-1H-indol-3-yl)-5-ethyl-thiazole-4-yl]-methanol (210 mg, 0.547 mmol), diisopropylethylamine (150 μl, 0.91 mmol) and dichloromethane (5 ml) under ice-water cooling and the resulting mixture was allowed to warm to room temperature slowly. Stirring was continued for 22 hours. The reaction mixture was quenched with 5% aqueous sodium carbonate (2 ml), and the aqueous layer extracted with dichloromethane (2×10 ml). The organic layers were combined, dried over magnesium sulfate, and concentrated in vacuo to yield the crude product. Flash column chromatography eluting with 10% acetone in n-heptane afforded 3-(4-chloromethyl-5-ethyl-thiazol-2-yl)-1-cyclohexylmethyl-7-methoxy-1H-indole (109 mg). Dimethylamine (2.2 M solution in tetrahydrofuran; 0.50 ml) was added to a mixture of 3-(4-chloromethyl-5-ethyl-thiazol-2-yl)-1-cyclohexylmethyl-7-methoxy-1H-indole (38 mg, 0.095 mmol), potassium carbonate (16 mg, 0.113 mmol) and sodium iodide (14 mg, 0.095 mmol) in acetonitrile (2 ml). The mixture was subjected to microwave irradiation for 5 min at 160° C., then partitioned between dichloromethane (20 ml) and 5% aqueous sodium carbonate (5 ml). The aqueous layer was extracted with dichloromethane (10 ml) and the combined organic layers were dried over magnesium sulfate and concentrated in vacuo. The resulting oil was dissolved in diethyl ether, then hydrogen chloride (1M solution in diethyl ether; 3 ml) was added to the solution. The resulting mixture was concentrated in vacuo to afford the title compound as a 1:1 hydrochloride salt (40 mg, 0.089 mmol). 1H NMR (400 MHz, CD3OD) δ 1.04-1.15 (2H, m), 1.16-1.30 (3H, m), 1.43 (3H, t, J 7.0), 1.55-1.78 (5H, m), 1.82-1.92 (1H, m), 3.05 (8H, m), 3.99 (3H, s), 4.33 (2H, d, J 7), 4.62 (2H, s), 6.91 (1H, d, J 8.0), 7.29 (1H, t, J 8.0), 7.62 (1H, d, J 8), 8.30 (1H, s). EIMS: m/z 412.3 [M+H]+, 367.0.

1. customirradiation for 5 min at 160° C.
2. custompartitioned between dichloromethane (20 ml) and 5% aqueous sodium carbonate (5 ml)
3. extractionThe aqueous layer was extracted with dichloromethane (10 ml)
4. dry with materialthe combined organic layers were dried over magnesium sulfate
5. concentrationconcentrated in vacuo
6. dissolutionThe resulting oil was dissolved in diethyl ether
7. additionhydrogen chloride (1M solution in diethyl ether; 3 ml) was added to the solution
8. concentrationThe resulting mixture was concentrated in vacuo

ORD record

ord-4bed5a8e31854b5d9847d73e7e5d621e

Source dataset

uspto-grants-2010_04

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07700634B2