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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033385Generated: October 31, 2026

Water → 3-amino-7-fluoro-1,3,4,5-tetrahydro-2H-1-benzazepin-2-on

https://huagongshe.com/reaction/1033385

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriphenylphosphineHCID 11776—
Reactant3-Azido-7-fluoro-2,3,4,5-tetrahydro-1H-1-benzazepin-2-oneHCID 53862901—
SolventTetrahydrofuranHCID 8028—
Product3-amino-7-fluoro-1,3,4,5-tetrahydro-2H-1-benzazepin-2-onHCID 5445859081%

Reaction Steps

3-Azido-7-fluoro-2,3,4,5-tetrahydro-1H-1-benzazepin-2-one (3.36 g, 15.3 mmol) (Step C) dissolved in dry tetrahydrofuran was treated with 4.00 g (15.3 mmol; leq) of triphenylphosphine and the resulting solution stirred at room temperature under nitrogen for 2 hours. Water (0.48 mL, 2eq) was added and the mixtured stirred at room temperature for 16 hours. Solvents were removed under vacuum and the residue purified by preparative HPLC on silica, eluting with methylene chloride/methanol (9:1) to afford 2.39 g (12.3 mmol, 81%) of product. 1H NMR (200MHz, CD3OD): 1.87 (m,1H), 2.41 (m,1H), 2.6-2.9 (m,2H), 3.30 (dd;8,12 Hz;1H), 7.0 (m,3H). FAB-MS: calculated for C10H11FN2O 194; found 195 (M+H,100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05310737
Source datasetuspto-grants-1994_05
ORD IDord-4fd1a3a423fe4118a6498ff14dfc08c2
Source noteuspto-grants-1994_05