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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 558297Generated: October 30, 2026

Phthalimide → HCID 21949925, compound

https://huagongshe.com/reaction/558297

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalimideHCID 6809—
ReactantTriphenylphosphineHCID 11776—
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
ReactantHCID 21949870HCID 21949870—
SolventTetrahydrofuranHCID 8028—
ProductAmmoniaHCID 222—
ProductHCID 21949925HCID 21949925152.2%

Reaction Steps

The alcohol from Example 202 (87 mg, 0.28 mmol), triphenylphosphine (220 mg, 0.84 mmol) and phthalimide (124 mg, 0.84 mmol) were dissolved in tetrahydrofuran (5 ml) at 0° C. under nitrogen and diisopropylazodicarboxylate (165 μl, 0.84 mmol) dissolved in tetrahydrofuran (1 ml) was added dropwise. The reaction was allowed to warm to room temperature and was stirred for 18 hours. The solvent was removed under reduced pressure, the residue was dissolved in ethanol (6 ml) and hydrazine hydrate (68 μl, 1.40 mmol) was added. The slurry was stirred for 48 hours at room temperature under nitrogen, concentrated under reduced pressure and the residue was dissolved in methanol. The solution was then passed through an SCX column eluting with methanol to remove impurities, then 2M ammonia in methanol solution to elute the product. The product was then purified by flash chromatography on silica gel eluting with dichloromethane:methanol (95:5) then dichloromethane:methanol:0.88 ammonia (90:10:1, by volume) to provide the title compound (67 mg) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063044B2
Source datasetuspto-grants-2011_11
ORD IDord-a5bd5bec28e24cae83a490f721ca9f6d
Source noteuspto-grants-2011_11