1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → N-[(5-fluoro-1-methylindole-2-carbonyl)valinyl]-3-amino-4-hydroxy-5-fluoropentanoic acid, t-butyl ester

온도

0 °C

DMAP (257 mg, 2.08 mmol) and EDAC (427 mg, 2.23 mmol) were added as solids to a solution of 5-fluoro-1-methylindole-2-carboxylic acid (359 mg, 86 mmol in 3 mL of DMF), and the resultant reaction mixture was stirred for 10 minutes under a nitrogen atmosphere at 0° C. N-(Valinyl)-3-amino-4-hydroxy-5-fluoropentanoic acid, t-butyl ester (579 mg, 1.86 mmol) in DMF (3 mL) was added and the resulting solution was stirred for 1 hour under a nitrogen atmosphere at 0° C. and 4 hours at room temperature. The reaction mixture was partitioned between ethyl acetate and 5% KHSO4 solution and the aqueous solution was back-extracted with ethyl acetate. The combined ethyl acetate solutions were washed with 5% KHSO4 solution, saturated sodium bicarbonate solution (2×) and brine, dried over sodium sulfate, and concentrated to give the title product as a slightly yellow solid (0.827 mg). TLC(methanol/methylene chloride, 1:9): Rf =0.52.

1. customthe resultant reaction mixture
2. stirringthe resulting solution was stirred for 1 hour under a nitrogen atmosphere at 0° C. and 4 hours at room temperature
3. customThe reaction mixture was partitioned between ethyl acetate and 5% KHSO4 solution
4. extractionthe aqueous solution was back-extracted with ethyl acetate
5. washThe combined ethyl acetate solutions were washed with 5% KHSO4 solution, saturated sodium bicarbonate solution (2×) and brine
6. dry with materialdried over sodium sulfate
7. concentrationconcentrated

ORD 기록

ord-2303058be115461db3cfdfa5c75e9206

출처 데이터셋

uspto-grants-1999_03

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US05877197