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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972745Generated: November 1, 2026

Trifluoroacetic acid → HCID 58529825, compound

https://huagongshe.com/reaction/1972745

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium CarbonateHCID 10340—
ReactantTriethylsilaneHCID 12052—
ReactantCarbonic acid, bis(1,1-dimethylethyl) esterHCID 10219638—
ReactantHCID 58529678HCID 58529678—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58529825HCID 5852982529%

Reaction Steps

To a cooled (0° C.) solution of tert-butyl 3-[(4-aminopyrrolo[2,1-f][1,2,4]triazin-7-yl)(hydroxy)methyl]azetidine-1-carboxylate (1.35 g, 4.25 mmol) in CH2Cl2 (12 mL) was added TFA (3.7 mL, 47.54 mmol) followed by triethylsilane (3.80 mL, 23.77 mmol), dropwise. The mixture was stirred at rt for 17 h. Additional TFA (1.8 mL) and triethylsilane (1.9 mL) were added and the mixture continued to stir at rt for 22 h. The reaction was concentrated to dryness. To a solution of the residue in THF (10 mL) was added 2M aqueous Na2CO3 (36 mL, 71.32 mmol) and di-tert-butyl carbonate (713 mg, 3.27 mmol). The mixture was stirred at rt for 17 h. The mixture was partitioned between EtOAc (50 mL) and H2O (25 mL) and the solid was removed by filtration. The layers of the filtrate were separated and the aqueous was further extracted with EtOAc (2×50 mL). The combined organics were washed with brine, dried (Na2SO4), and concentrated to dryness. The crude residue was purified by ISCO® chromatography using a gradient of 50 to 75% ethyl acetate in hexanes to afford 259 mg (29%) of the desired product. ES-MS m/z 304.02 [M+H]+, HPLC RT (min) 2.35.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431695B2
Source datasetuspto-grants-2013_04
ORD IDord-d69adf9dfd404b2891c43cef64e4351e
Source noteuspto-grants-2013_04