Allyl Alcohol → 7-Allyloxy-3-(4-chlorophenyl)-2-(2-chlorophenyl)-pyrazolo[1,5-a]pyrimidine

Participants

Reaction Steps

To a suspension of 7-chloro-3-(4-chlorophenyl)-2-(2-chlorophenyl)-pyrazolo[1,5-a]pyrimidine (I-13A-1a; 30 mg, 0.08 mmol) in allyl alcohol (0.8 ml) was added NaH (60% dispersion in oil, 2 mg, 0.08 mmol). After stirring overnight, the reaction was concentrated and purified on a Chromatotron using methylene chloride as eluant to give product 13A-1 (12 mg, 38%) as a solid: +ESI MS (M+1) 396.4; 1H NMR (400 MHz, CD3OD) δ 8.51 (d, J=5.4 Hz, 1H), 7.53–7.40 (m, 6H), 7.24 (d, J=8.7 Hz, 2H), 6.68 (d, J=5.4 Hz, 1H), 6.20 (ddt, J=17.0, 10.4, 5.8 Hz, 1H), 5.64–5.58 (m, 1H), 5.45–5.41 (m, 1H), 5.10–5.08 (m, 2H).

Provenance & Evidence