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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2188243Generated: October 29, 2026

Hydrazine hydrate (1:1) → HCID 88158463, compound

https://huagongshe.com/reaction/2188243

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantTetrahydrofuran ethanolHCID 21873804—
ReactantHCID 88158466HCID 88158466—
SolventTetrahydrofurane dichloromethaneHCID 21919333—
ProductHCID 88158463HCID 88158463—

Reaction Conditions

Temperature25 °C

Reaction Steps

A suspension of Example 1D (2.45 g) in 1:1 THF/ethanol (36 mL) was heated to 70 ° C., and treated with hydrazine monohydrate (3×227 μL) at 1 hour intervals. One hour after the final addition, the mixture was cooled to 25° C., and filtered. The filtrate was concentrated, dissolved in a mixture of pyridine (10 mL) and dichloromethane (25 mL), cooled to −5° C., treated with acetic anhydride (880 μL), warmed to room temperature, stirred for 5 minutes, and concentrated to provide crude product. The crude product was dissolved in 4:1 THF/dichloromethane (75 mL) and washed with 1:1 brine/water. The aqueous wash was extracted with dichloromethane (25 mL), and the combined extracts were dried over MgSO4. Next the mixture was filtered and concentrated. The residue was dissolved in acetone (20 mL) and filtered. The filtrate was concentrated and the residue triturated with hexanes to provide the desired product. mp 177-179° C.; MS (ESI(+)) m/e 437 (M+H)+; 1H NMR (300 MHz, CDCl3) δ 7.81 (t, 1H), 7.50 (s, 1H), 7.47 (dd, 1H), 7.20 (dd, 1H), 5.92 (br t, 1H), 4.80 (m, 1H), 4.06 (t, 1H), 3.77 (dd, 1H), 3.75-3.55 (m, 2H), 2.02 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06410728B1
Source datasetuspto-grants-2002_06
ORD IDord-516689d4c0d64834be9fc6ce23c0c838
Source noteuspto-grants-2002_06