HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1399090Generated: October 31, 2026
Lithium borohydride → {9-Chloro-1-[6-(dimethylamino)-2-methylpyridin-3-yl]-1,2,3,4-tetrahydropyrimido[1,2-a]benzimidazol-6-yl}methanol
https://huagongshe.com/reaction/1399090
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | Methyl 9-chloro-1-[6-(dimethylamino)-2-methylpyridin-3-yl]-1,2,3,4-tetrahydropyrimido[1,2-a]benzimidazole-6-carboxylate | HCID 57786114 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | {9-Chloro-1-[6-(dimethylamino)-2-methylpyridin-3-yl]-1,2,3,4-tetrahydropyrimido[1,2-a]benzimidazol-6-yl}methanol | HCID 57785958 | 100% |
Reaction Steps
Lithium borohydride (74.3 mg, 3.41 mmol) was added to a stirred solution of methyl 9-chloro-1-[6-(dimethylamino)-2-methylpyridin-3-yl]-1,2,3,4-tetrahydropyrimido[1,2-a]benzimidazole-6-carboxylate (341 mg, 0.853 mmol) in tetrahydrofuran (5.0 mL) at room temperature, and the mixture was stirred at 40° C. for 20 hr. The reaction was quenched by aqueous saturated ammonium chloride at 0° C., concentrated in vacuo and the precipitate was collected by filtration, washed with water, diisopropyl ether to give the title compound as a colorless powder (317 mg, 0.853 mmol, 100%).
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-12fca15b515549cba4714b760bd2ea56 |
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| Source note | uspto-grants-2014_12 |
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