HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2366241Generated: November 2, 2026
Lithium borohydride → (6-Aminopyrimidin-4-yl)methanol
https://huagongshe.com/reaction/2366241
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | Methyl 6-aminopyrimidine-4-carboxylate | HCID 21955432 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (6-Aminopyrimidin-4-yl)methanol | HCID 21934615 | 61.5% |
Reaction Steps
To a stirred solution of methyl 6-aminopyrimidine-4-carboxylate (2.0 g, 13 mmol) in MeOH (20 mL) at 25° C., was added LiBH4 (0.85 g, 39 mmol). After addition, the resulting mixture was allowed to stir at 70° C. for 16 hours. TLC indicated the starting material was consumed completely at this point. Solvents were removed under reduced pressure and the residue was purified via chromatography column on silica gel eluting with a 5% gradient of methanol in dichloromethane to give the desired alcohol as pale yellow oil (1.0 g, 61% yield). LCMS (ESI) m/z: 126.1 [M+H+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08697708B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-4844b7b696b44e889a7cf08ae9bb0d30 |
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| Source note | uspto-grants-2014_04 |
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