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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 47694Generated: October 28, 2026

Potassium Carbonate → Methyl 4-((2s)-2-{[(tert-butoxycarbonyl)((2s)-2-{[tert-butyl(dimethyl)silyl]oxy}-3-phenoxypropyl)amino]methyl}-3,4-dihydro-2h-chromen-6-yl)-2-hydroxybenzoate

https://huagongshe.com/reaction/47694

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactanttert-butyl (2S)-2-{[tert-butyl(dimethyl)silyl]oxy}-3-phenoxypropyl{[(2S)-6-(2,2-dimethyl-4-oxo-4H-1,3-benzodioxin-7-yl)-3,4-dihydro-2H-chromen-2-yl]methyl}carbamateHCID 86587740—
SolventMethanolHCID 887—
ProductMethyl 4-((2s)-2-{[(tert-butoxycarbonyl)((2s)-2-{[tert-butyl(dimethyl)silyl]oxy}-3-phenoxypropyl)amino]methyl}-3,4-dihydro-2h-chromen-6-yl)-2-hydroxybenzoateHCID 6989594597%

Reaction Steps

To a solution of Example 204 (0.8 g, 1.14 mmol, 1.0 eq.) in methanol (10 mL) was added potassium carbonate (0.078 g, 0.57 mmol, 0.5 eq.) at room temperature. The reaction mixture was allowed to stir at room temperature for 18 hours and then concentrated under reduced pressure. The resulting residue was washed with distilled water (10 mL) and extracted with ethyl acetate (3×10 mL). The combined extracts were dried over magnesium sulfate, filtered and concentrated under reduced pressure to afford the desired product as pale yellow oil (0.75 g, 97%). 1H NMR (CDCl3) δ10.68 (s, 1 H), 7.73 (d, 1H), 7.26-7.14 (m, 4H), 6.94 (dd, 1H), 6.86-6.75 (m, 5H), 4.21-4.02 (m, 2H), 3.83 (s, 3H), 3.80-3.56 (m, 4H), 3.40-3.21 (m, 2H), 2.80-2.67 (m, 2H), 1.95-1.92 (m, 1H), 1.65-1.60 (m, 1H), 1.38 (s, 9H), 0.83 (s, 9H), 0.001 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06699860B2
Source datasetuspto-grants-2004_03
ORD IDord-479d7073bf434ca5af8b75d104644ba6
Source noteuspto-grants-2004_03