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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 132815Generated: October 30, 2026

Acetic Acid → HCID 16754249, compound

https://huagongshe.com/reaction/132815

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantAcetoneHCID 180—
ReactantWaterHCID 962—
ReactantTrifluoroacetateHCID 84468—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 67527009HCID 67527009—
SolventTetrahydrofuranHCID 8028—
ProductHCID 16754249HCID 1675424943%

Reaction Conditions

Temperature55 °C

Reaction Steps

To a solution of morpholin-4-yl-[5-(morpholin-2-ylmethoxy)-1-(2,2,2-trifluoro-ethyl)-1H-indol-2-yl]-methanone as trifluoroacetate salt (example 1, step 2, 120 mg, 1.0 eq.) in tetrahydrofuran (2 mL) were successively added water (0.004 mL, 1.1 eq.), acetone (0.019 mL, 1.5 eq.), acetic acid (0.040 mL, 3.0 eq.) and a solution of sodium cyanoborohydride in tetrahydrofuran (1M, 0.33 mL, 1.5 eq.). The reaction mixture was stirred at 55° C. overnight and concentrated in vacuo. Water (5 mL) and hydrochloric acid (1N, 1.5 mL) were added to the residue and the solution was washed with ethyl acetate and then basified by addition of an aqueous solution of potassium carbonate. The aqueous fraction was extracted with ethyl acetate and the combined organic layers were washed with brine. The organic residue was purified on silica, eluting with 98:2 dichloromethane/methanol, to yield 45 mg (43%) of the desired product as white foam. MS (m/e): 470.5 (MH+, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07388095B2
Source datasetuspto-grants-2008_06
ORD IDord-3ebeae3676fa4aba9336e9001c70eb6a
Source noteuspto-grants-2008_06