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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2362638Generated: November 1, 2026

Acetic Acid → HCID 67003833, compound

https://huagongshe.com/reaction/2362638

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDimethylamineHCID 674—
ReactantSodium SulfateHCID 24436—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 86659280HCID 86659280—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67003833HCID 67003833—

Reaction Steps

To a solution of 2-(4-(5-chloro-4-(2-(1-(methoxymethoxy)cyclobutyl)thiazol-5-yl)-1-tosyl-1H-pyrrolo[2,3-b]pyridin-2-yl)-1H-pyrazol-1-yl)acetaldehyde (14C) (300 mg, 0.490 mmol) in tetrahydrofuran (3.267 mL) was added sequentially acetic acid (0.056 mL, 0.980 mmol), sodium sulfate (139 mg, 0.980 mmol) and dimethylamine (0.368 mL, 0.735 mmol). The reaction was stirred for 0.5 hours at ambient temperature, and sodium triacetoxyborohydride (208 mg, 0.980 mmol) was added in a single portion. The reaction was stirred overnight and then quenched by the addition of saturated aqueous sodium bicarbonate and ethyl acetate. The layers were separated, and the aqueous layer was extracted with addition ethyl acetate (2×). The combined organics were dried with anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give the title compound, which was used in the next step without further purification. MS ESI(+) m/z 641.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691810B2
Source datasetuspto-grants-2014_04
ORD IDord-2facb2494be54bbd8b3d337d2515a0dd
Source noteuspto-grants-2014_04