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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1424095Generated: November 2, 2026

Sodium Bicarbonate → 6-(4-{1-[(8R)-8-(Hydroxymethyl)-8-methyl-5,6,8,9-tetrahydro[1,2,4]triazolo[4,3-d][1,4]thiazepin-3-yl]cyclopropyl}phenyl)nicotinonitrile

https://huagongshe.com/reaction/1424095

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant6-(4-{1-[(8R)-8-({[t-Butyl(dimethyl)silyl]oxy}methyl)-8-methyl-5,6,8,9-tetrahydro[1,2,4]triazolo[4,3-d][1,4]thiazepin-3-yl]cyclopropyl}phenyl)nicotinonitrileHCID 86712943—
SolventTetrahydrofuranHCID 8028—
Product6-(4-{1-[(8R)-8-(Hydroxymethyl)-8-methyl-5,6,8,9-tetrahydro[1,2,4]triazolo[4,3-d][1,4]thiazepin-3-yl]cyclopropyl}phenyl)nicotinonitrileHCID 8671294471.2%

Reaction Steps

The compound (375 mg, 0.70 mmol) obtained in Example 61-1) was dissolved in tetrahydrofuran (7 mL). Tetrabutylammonium fluoride (1.0 mol/L tetrahydrofuran solution, 0.84 mL, 0.84 mmol) was added to the solution at room temperature, and the mixture was stirred at room temperature for 1 h under a nitrogen atmosphere. Saturated aqueous sodium hydrogencarbonate (10 mL) was added to the reaction mixture, and the mixture was extracted with ethyl acetate (50 mL). The organic layer was washed with saturated sodium chloride solution and then dried with anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the obtained residue was purified by silica gel column chromatography (elution solvent: methanol/ethyl acetate=10% to 40%) to obtain the title compound (208 mg, 71%) in a white solid form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927536B2
Source datasetuspto-grants-2015_01
ORD IDord-5fba7edd33ee4cb6ae6edcddf7f9aad4
Source noteuspto-grants-2015_01