Dimethylformamide → HCID 22638736, compound

Temperature

-78 °C

Oxalyl chloride (0.5 ml of 2.0 M solution in methylene chloride, 1.0 mmol) was diluted with dry methylene chloride (5.0 ml) and cooled to −78° C. under a nitrogen atmosphere. DMF (0.08 ml, 1.12 mmol) was added via a micro syringe and the solution was stirred at −78° C. for 10 min. A solution of 3-[2-(2-hydroxy-ethyl)-cyclopropyl]-1-(toluene-4-sulfonyl)-1H-indole-5-carbonitrile (250 mg, 0.657 mmol) in dry methylene chloride (5 ml) was added drop wise, and the solution was stirred at −78° C. for 1 hr, and then triethylamine (1.0 ml) was added. The solution was concentrated in vacuo, and the residue was dissolved in ethyl acetate (10 ml). The ethyl acetate solution was extracted with HCl (5 ml of 1 N solution), and with brine (5 ml). The ethyl acetate solution was dried over sodium sulfate and concentrated in vacuo. The residue was chromatographed on silica gel using methylene chloride as the eluent to give 3-[2-(2-oxo-ethyl)-cyclopropyl]-1-(toluene-4-sulfonyl)-1H-indole-5-carbonitrile (167 mg, 67%). 1H NMR (500 MHz, CDCl3): δ9.87 (s, 1H), 8.03 (d, 1H), 7.96 (s, 1H), 7.74 (d, 2H), 7.56(d, 1H), 7.35 (s, 1H), 7.25 (d, 2H), 2.59 (m, 2H), 2.36 (s, 3H), 1.67 (m, 1H), 1.30 (m, 1H), 1.30 (m, 1H), 1.02 (m, 1H), 0.89(m, 1H). MS m/e 379.16 (MH+).

1. stirringthe solution was stirred at −78° C. for 1 hr
2. concentrationThe solution was concentrated in vacuo
3. dissolutionthe residue was dissolved in ethyl acetate (10 ml)
4. extractionThe ethyl acetate solution was extracted with HCl (5 ml of 1 N solution)
5. dry with materialThe ethyl acetate solution was dried over sodium sulfate
6. concentrationconcentrated in vacuo
7. customThe residue was chromatographed on silica gel

ORD record

ord-96f418e903434977afb4f6bdd865b53a

Source dataset

uspto-grants-2004_08

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US06777437B2