HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013903Generated: October 25, 2026
Lithium borohydride → HCID 178418978, compound
https://huagongshe.com/reaction/1013903
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | HCID 178418985 | HCID 178418985 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178418978 | HCID 178418978 | — |
Reaction Steps
To a solution of [6-methoxycarbonyl-2-(4-propionylamino-phenyl-sulfanyl)-pyrimidin-4-yl]-(5-methyl-2H-pyrazol-3-yl)-amine (2g, 4.85 mmol) in THF (100 mL) is added lithium borohydride (0.32 g, 14.5 mmol). The reaction mixture is stirred at 50° C. for 1.5 hours. The reaction is then quenched with dilute HCl and extracted with ethyl acetate. The organic layer is successively washed with aqueous saturated NaHCO3 and brine, dried over MgSO4 and evaporated. The solid residue is triturated in ethyl acetate and the resulting white solid is collected by filtration to give the desired product [6-hydroxymethyl-2-(4-propionylamino-phenyl-sulfanyl)-pyrimidin-4-yl]-(5-methyl-2H-pyrazol-3-yl)-amine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07982037B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-1123abcfb99e41059ef0ed532555f23b |
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| Source note | uspto-grants-2011_07 |
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