Azetidine → HCID 57159919, compound

Participants

Reaction Steps

(+)-(1S, 2R, 4R)-4-(2-Amino-6-chloro-9H-purin-9-yl)-2-(hydroxymethyl)cyclopentanol (340 mg, 1.20 mmol) and azetidine (98%, ALdrich, 1.0 mL) and methanol (6 mL) were maintained at 60° C. in a sealed tube for 18 hours. To the cooled solution was added 1N sodium hydroxide (1.2 mL). Volatiles were evaporated and the residue chromatographed on silica gel. Title compound was eluted with methanol: ethyl acetatel 15:85 as a white foam which solidified to white powder from methanol-acetonitrile (333 mg, 91%), mp 194°-195°; mass spectrum (Cl, CH4) 305 (M+1)- ; 1H-NMR (DMSO-d6)δ: 7.81 (s, 1, H8), 5.88 (br s, 2, NH2), 495-4.80 (m. 1, CH-N), 4.76 (d, J=3.9 Hz, 1, OH),4.66 (t, J=5.0 Hz, 1, CH2 -OH). 4.4-4.15(br m, 4, 2CH2N), 4.10-4.0 (m, 1, CHO), 3.6-3.4 (m, 2, CH2O), 2.5-1.9 (m, 6, methylene), 1.75-1.5 (m, 1, 1/2CH2):[α]20589 +10.1°,[α]20578 +10.7°, [α]20540 +11.9°, [α]20436 +18.3°, [α]20356 +25.2°(c=0.812, methanol).

Provenance & Evidence