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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2216615Generated: October 30, 2026

HCID 21057704, compound → HCID 68685067, compound

https://huagongshe.com/reaction/2216615

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 21057704HCID 21057704—
ReactantHCID 21057710HCID 21057710—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68685067HCID 68685067—

Reaction Steps

To the mixture [21.2 g (0.11 mol)] of 2,3-dihydropyrazolo[5,1-b]thiazol-6-carboxylic acid ethyl ester and 2,3-dihydropyrazolo[5,1-b]thiazol-7-carboxylic acid ethyl ester in 540 ml of dry tetrahydrofuran was added LiAlH4 (4.05 g, 0.11 mol) under a nitrogen atmosphere at 0° C., and then stirred for 2.5 hours at room temperature. The mixture was quenched with water (15 ml) and the precipitate was filtered through a pad of Celite. The pad was washed with water (100 ml) and tetrahydrofuran (500 ml). The filtrate was concentrated under reduced pressure, and then water (150 ml) was added. The aqueous layer was extracted with dichloromethane (15×250 ml). The combined organic layers were dried (MgSO4) and filtered. The filtrate was concentrated under reduced pressure and a mixture of (2,3-dihydropyrazolo[5,1-b]thiazol-6-yl) methanol and (2,3-dihydropyrazolo[5,1-b]thiazol-7-yl) methanol was obtained as pale brown oil (15.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07112582B2
Source datasetuspto-grants-2006_09
ORD IDord-38cef1393c304736b6e3320c16cb2c7b
Source noteuspto-grants-2006_09