Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Sulfate | HCID 24436 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 67323323 | HCID 67323323 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 53311621 | HCID 53311621 | — |
Reaction Steps
90 mg (0.171 mmol) of 3,3-dimethyl-4-oxo-5-{4-[4-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalen-2-yl)thiazol-2-yl]piperazin-1-yl}pentanoic acid ethyl ester from step a was dissolved in 8 ml of THF. 1.71 ml (1.71 mmol) of a 1M lithium aluminium hydride solution in THF was added dropwise with ice-cooling. The mixture was stirred for a further 1 h with cooling, then stirred at room temperature and subsequently at 40° C. overnight, decomposed using a saturated sodium sulfate solution with cooling and extracted twice with EA. The organic phase was washed with a saturated sodium chloride solution, dried over sodium sulfate, filtered, evaporated to dryness and purified by means of preparative HPLC. The product is in the form of the hydrochloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08907098B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-85f449b815434694bd8dd315cd131de2 |
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| Source note | uspto-grants-2014_12 |
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