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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2114510Generated: October 31, 2026

Trifluoroacetic acid → Trifluoroacetic acid

https://huagongshe.com/reaction/2114510

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantN,N,N-Trimethylmethanaminium tetrahydroborateHCID 28122—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 11711042HCID 11711042—
ReactantHCID 178419906HCID 178419906—
Solvent1,2-DichloroethaneHCID 11—
SolventTetrahydrofuranHCID 8028—
ProductTrifluoroacetic acidHCID 6422—
ProductHCID 11719932HCID 11719932—

Reaction Steps

Using an adaptation of the method described in Procedure 7, substituting N-[2-(10-piperidin-4-yl-10H-phenoxazin-3-yl)-phenyl]-acetamide, 2j for the TFA salt of 10-piperidin-4-yl-3-(1H-tetrazol-5-yl)-10H-phenoxazine, 6a, sodium triacetoxyborohydride for tetramethylammonium borohydride, and a 3:1 mixture of 1,2-dichloroethane:THF for 100% 1,2-dichloroethane, the title compound N-(2-{10-[1-(1H-imidazol-2-ylmethyl)-piperidin-4-yl]-10H-phenoxazin-3-yl}-phenyl)-acetamide, 7j was obtained as a TFA salt after purification via reverse phase HPLC (eluent: CH3CN in H2O containing 0.1% TFA). MS m/z (MH+) 479.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07432257B2
Source datasetuspto-grants-2008_10
ORD IDord-fc6795bdaa284192a9db13338bbb28e9
Source noteuspto-grants-2008_10