HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 398468Generated: October 29, 2026
Tetrahydrofuran → HCID 22315240, compound
https://huagongshe.com/reaction/398468
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 20707093 | HCID 20707093 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Product | HCID 22315240 | HCID 22315240 | 55.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06610846B1 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-e78e1452155a4b12a6dbd22cb1dd0f84 |
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| Source note | uspto-grants-2003_08 |
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