HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2216615Generated: October 30, 2026
HCID 21057704, compound → HCID 68685067, compound
https://huagongshe.com/reaction/2216615
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 21057704 | HCID 21057704 | — |
| Reactant | HCID 21057710 | HCID 21057710 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68685067 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07112582B2 |
|---|
| Source dataset | uspto-grants-2006_09 |
|---|
| ORD ID | ord-38cef1393c304736b6e3320c16cb2c7b |
|---|
| Source note | uspto-grants-2006_09 |
|---|