2,2-Dimethoxypropane → {(3aR,4R,6R,6aS)-6-[(6-Chloropyrimidin-4-yl)amino}-2,2-dimethyltetrahydro-3aH-cyclopenta[d][1,3]dioxol-4-yl]methanol

A solution of (1R,2S,3R,5R)-3-[(6-chloropyrimidin-4-yl)amino]-5-(hydroxymethyl)cyclopentane-1,2-diol (255 mg, 0.982 mmol), p-toluenesulfonic acid monohydrate (187 mg, 0.982 mmol) and 2,2-dimethoxypropane (0.670 mL, 0.545 mmol) in MeOH (5.00 mL) was stirred overnight. The reaction was quenched via addition of saturated aqueous NaHCO3 solution (10 mL) and MeOH was removed in vacuo. The aqueous mixture was extracted with DCM (4×20 mL) and the combined organics were concentrated in vacuo. The crude mixture was purified via silica gel chromatography eluting with a gradient of 0 to 10% MeOH in DCM to afford the title compound (135 mg, 45.8%). LC/MS: Rt=1.77 min, ES+ 300. (AA standard).

1. customThe reaction was quenched via addition of saturated aqueous NaHCO3 solution (10 mL) and MeOH
2. customwas removed in vacuo
3. extractionThe aqueous mixture was extracted with DCM (4×20 mL)
4. concentrationthe combined organics were concentrated in vacuo
5. customThe crude mixture was purified via silica gel chromatography
6. washeluting with a gradient of 0 to 10% MeOH in DCM

ORD-Eintrag

ord-ae36477bf1f24cd185e14d70498ead5b

Quelldatensatz

uspto-grants-2013_07

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US08481550B2