HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 861353Generated: October 30, 2026
Aluminium lithium hydride → HCID 70200310, compound
https://huagongshe.com/reaction/861353
Participants
| Role | Name | HCID | Charge |
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| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 57016126 | HCID 57016126 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 70200310 | HCID 70200310 | 63% |
Reaction Steps
A solution of 0.13 g (0.33 mmol) of (7S,8aS)-7-(4-((methoxycarbonyl)methyl)phenoxy)methyl-2-(5-fluoropyrimidin-2-yl)-1,2,3,4,6,7,8,8a-octahydro-pyrrolo[1,2-a]pyrazine (Example 11i) in 15 mL of anhydrous ethyl ether was added dropwise to an ice-cold suspension of 0.025 g (0.65 mmol) of lithium aluminum hydride in 15 mL of anhydrous ethyl ether and the mixture stirred for 30 min. The reaction was carefully quenched at 0° C. with 0.025 mL of water, 0.025 mL of 15% sodium hydroxide, and 0.075 mL of water. The precipiate which formed was filtered through Celite, the filtrate concentrated in vacuo, and purification of the residue by flash silica gel chromatography with 95:5 ethyl acetate:methanol gave 0.075 g (63%) of the title compound. mp (.HCl) 145°-147° C. HRMS calcd for C20H26FN4 O2 (MH+): 373.2040, found: 373.2054.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05714487 |
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| Source dataset | uspto-grants-1998_02 |
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| ORD ID | ord-12b82b0127504299966061e250f6691f |
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| Source note | uspto-grants-1998_02 |
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