2,6-Dimethylmorpholine, cis- → HCID 58075491, compound

Participants

Reaction Steps

2,4-dichloro-7-(4-fluorophenyl)-5,7-dihydrofuro[3,4-d]pyrimidine (Preparation M) was reacted as described in Preparation Xa with (2R,6S)-2,6-dimethylmorpholine to give 2-chloro-4-((2S,6R)-2,6-dimethylmorpholino)-7-(4-fluorophenyl)-5,7-dihydrofuro[3,4-d]pyrimidine (Preparation Mh). LC-MS (M+H)+=364.2. 1H NMR (500 MHz, CDCl3) δ ppm 7.39 (dd, J=8.70, 5.34 Hz, 2 H) 7.07 (t, J=8.70 Hz, 2 H) 5.90 (br. s., 1 H) 5.34-5.42 (m, 1 H) 5.24-5.34 (m, 1 H) 4.14 (q, J=7.02 Hz, 2 H) 3.67 (ddd, J=10.38, 6.41, 2.44 Hz, 4 H), 1.20 (m, 6 H).

Provenance & Evidence