HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1399059Generated: October 30, 2026
Lithium borohydride → HCID 57785948, compound
https://huagongshe.com/reaction/1399059
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | HCID 57785993 | HCID 57785993 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57785948 | HCID 57785948 | 87% |
Reaction Steps
Lithium borohydride (2.14 g, 98.1 mmol) was added to a stirred solution of methyl 9-chloro-1-[4-chloro-2-(trifluoromethyl)phenyl]-1,2,3,4-tetrahydropyrimido[1,2-a]benzimidazole-6-carboxylate (10.9 g, 24.5 mmol) in tetrahydrofuran (80 mL) at room temperature, and the mixture was stirred at room temperature for 12 hr and at 50° C. for 4 hr. The reaction was quenched by methanol, and the mixture was diluted with aqueous saturated ammonium chloride at 0° C. and extracted with ethyl acetate. The combined organic layer was washed with brine, dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo. The residue was washed with ethyl acetate/diisopropyl ether to give the title compound as a colorless powder (8.81 g, 21.2 mmol, 87%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08901141B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-9bab74ca1df146288e1b305809cf815e |
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| Source note | uspto-grants-2014_12 |
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