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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1489000Generated: November 2, 2026

Water → HCID 15896060, compound

https://huagongshe.com/reaction/1489000

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 0.1M 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) δ8.05 (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) ν3136, 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 numberUS05677302
Source datasetuspto-grants-1997_10
ORD IDord-a26f56cb5d834849893fe21fd872a38b
Source noteuspto-grants-1997_10