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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289603Generated: November 1, 2026

Water → HCID 15896060, compound

https://huagongshe.com/reaction/2289603

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 10130628HCID 10130628—
SolventMethanolHCID 887—
ProductHCID 15896060HCID 15896060—

Reaction Steps

To a suspension of 3-(1-oxoethyl)-1,2,4-thiadiazolo[4,5-a]benzimidazole (729 mg, 3.36 mmol) in 200 mL methanol, was added sodium borohydride (140 mg, 3.69 mmol). The mixture was stirred for 30 min and 0.1 mL of water was added. The methanol was evaporated and the residue was partitioned between ethyl acetate and 0.1 M hydrochloric acid. The aqueous phase was extracted with ethyl acetate. The organic phases were combined, washed twice with brine, dried and evaporated. The crude residue was purified by chromatography using chloroform/methanol to give 3-(1-hydroxyethyl)-1,2,4-thiadiazolo[4,5-a]benzimidazole. mp 174-175° C.; 1H NMR (CDCl3) δ 8.05 (d, 1H), 7.80 (d, 1H), 7.47 (td, 1H), 7.36 (td, 1H), 5.39 (q, 1H), 2.76 (d, 1H), 1.84 (d, 3H) ppm; IR (KBr) ν 3136, 1544, 1494, 1478, 1451, 1374, 1250, 1200, 1123, 1103, 1093, 752, 729, 711 cm-1 ; MS m/z 219 (M+), 148 (M+ -CH3CH(OH)CN)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06093738
Source datasetuspto-grants-2000_07
ORD IDord-7f202c7d7a184d6ab4e62a1abc8abfec
Source noteuspto-grants-2000_07