Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1011588Generated: November 2, 2026

Tetrahydrofurfuryl alcohol → HCID 25003273, compound

https://huagongshe.com/reaction/1011588

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofurfuryl alcoholHCID 7360—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 25003272HCID 25003272—
SolventAmmonium ChlorideHCID 25517—
ProductHCID 25003273HCID 2500327337%

Reaction Steps

Sodium borohydride (18 mg, 0.48 mmol) was added to a solution of 2-aminocarbonylamino-5-(3-chlorophenyl)-4-formylpyrrole-3-carboxamide (Compound No. 17-1, 50 mg, 0.16 mmol) in the mixed solvent (tetrahydrofuran methanol=2:1, 1.5 mL) and the mixture was stirred at room temperature for 4 hours. Saturated aqueous ammonium chloride solution (50 mL) was added to the reaction solution, extracted with ethyl acetate (50 mL). The organic layer was dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The obtained solid was washed with chloroform (15 mL) and dried under reduced pressure to give the target compound (19 mg) as an orange solid (Yield 37%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977371B2
Source datasetuspto-grants-2011_07
ORD IDord-8d8e384063eb4b13aecec554da2a1688
Source noteuspto-grants-2011_07