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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 398468Generated: October 29, 2026

Tetrahydrofuran → HCID 22315240, compound

https://huagongshe.com/reaction/398468

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 20707093HCID 20707093—
ReactantAluminium lithium hydrideHCID 21226445—
ProductHCID 22315240HCID 2231524055.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 2-[2-(4-chloro-phenyl)-3-cyclopentyl-propionylamino]-thiazole-4-carboxylic acid methyl ester (prepared as in Example 32, 127.7 mg, 0.31 mmol) in tetrahydrofuran (0.4 mL) was added to a slurry of lithium aluminum hydride (15.0 mg, 0.39 mmol) in tetrahydrofuran (2.24 mL) at 0° C. The reaction mixture was stirred at 0° C. for 2 h. The reaction was then quenched by the dropwise addition of water. The reaction was then diluted with more water (25 mL) and extracted with ethyl acetate (3×25 mL). The combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 230-400 mesh, 75/25 hexanes/ethyl acetate) afforded 2-(4-chloro-phenyl)-3-cyclopentyl-N-(5-hydroxymethyl-thiazol-2-yl)-propionamide (63.4 mg, 55.4%) as a white solid: mp 115-117° C.; EI-HRMS m/e calcd for C18H21ClN2O2S (M+) 364.1012, found 364.1004.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610846B1
Source datasetuspto-grants-2003_08
ORD IDord-e78e1452155a4b12a6dbd22cb1dd0f84
Source noteuspto-grants-2003_08