1,3-Diethyl 2-oxopropanedioate → 1-Ethyl-5-trifluoromethanesulfonyl-1H-benzoimidazole-2-carboxylic acid

온도

40 °C

N1-Ethyl-4-trifluoromethanesulfonyl-benzene-1,2-diamine (134 mg, 0.50 mmol) and 2-oxo-malonic acid diethyl ester (91 μL, 1.2 equiv) were dissolved in 0.7 mL dry pentanol and heated to reflux for 24 h. The reaction mixture was then evaporated by blowing with a stream of nitrogen while heating, the oil was then placed under full vacuum for at least 20 h whereupon a low melting solid began to form. 1-Ethyl-5-trifluoromethanesulfonyl-1H-benzoimidazole-2-carboxylic acid pentyl ester 1HNMR (400 MHz, d6-DMSO) δ 8.52 (d, J=2.0 Hz, 1H), 8.30 (dd, J=9.2, 2.0 Hz, 1H), 8.07 (d, J=9.2 Hz, 1H), 4.37 (t, J=6.6 H 4.31 (q, J=7.2 Hz, 2H), 1.71 (m, 2H), 1.37 (m, 4H), 1.27 (t, J=7.4 Hz, 3H), 0.89 (T, J=7.0 Hz, 3H); LCMS-APCI m/z 393 [M+1]+. This pentyl ester was used directly (85 mg, 0.217 mmol) and dissolved in warm ethanol (3 mL) with the addition of 1 M sodium hydroxide (1 mL). The reaction mixture was warmed to 40° C. and stirred for 2 h. The reaction mixture was then partially evaporated by blowing with a stream of nitrogen and transferred to a vial containing chloroform and water. The two phases were shaken together, the organic phase was removed, and the process repeated once with additional chloroform. To the aqueous phase was added ethyl acetate, the mixture was acidified with 3 M aqueous hydrochloric acid to pH 2.5, and the organic phase was separated, washed with saturated brine, dried (Na2SO4) and evaporated to yield the acid 42: 1HNMR (400 MHz, d6-DMSO) 8 14.3 (br s, 1H), 8.51 (d, J=2.35 Hz, 1H), 8.30 (dd, J=9.06, 2.28 Hz, 1H), 8.07 (d, J=9.09 Hz, 1H), 4.31 (q, J=7.14 Hz, 2H), 1.28 (t, J=7.10 Hz, 3H); LCMS-APCI m/z [M−1]− 321.

1. temperatureheated
2. temperatureto reflux for 24 h
3. customThe reaction mixture was then evaporated
4. temperaturewhile heating
5. waitthe oil was then placed under full vacuum for at least 20 h whereupon a low melting solid
6. customto form
7. customThe reaction mixture was then partially evaporated
8. additiona vial containing chloroform and water
9. stirringThe two phases were shaken together
10. customthe organic phase was removed
11. additionTo the aqueous phase was added ethyl acetate
12. customthe organic phase was separated
13. washwashed with saturated brine
14. dry with materialdried (Na2SO4)
15. customevaporated

ORD 기록

ord-4205891017db4edc87222456fef41976

출처 데이터셋

uspto-grants-2003_07

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US06596772B1