HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1106534Generated: October 30, 2026
Sodium borohydride → HCID 18789140, compound
https://huagongshe.com/reaction/1106534
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 18789027 | HCID 18789027 | — |
| Catalyst | Palladium Chloride | HCID 24290 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 18789140 | HCID 18789140 | 40.4% |
Reaction Steps
In a mixed solvent of 300 ml of tetrahydrofuran and 150 ml of methanol were dissolved 11.30 g of 8-tert-butyl-5-chloro-6,7-dihydro-8H-pyrrolo[3,2-e]pyrazolo-[1,5-a]pyrimidine, and the reaction system was cooled to 0° C. To the solution were gradually added 3.75 g of palladium chloride and 7.83 g of sodium borohydride, and the mixture was stirred for 30 minutes at 0° C. Furthermore, 7.50 g of palladium chloride and 5.66 g of sodium borohydride were gradually added, and the resultant mixture was stirred for 30 minutes at 0° C. and for 2 hours at room temperature. The reaction solvent was distilled off under reduced pressure, and the resultant crude product was subjected to column chromatography on silica gel (ethyl acetate→ethyl acetate:methanol=10:1) to obtain 3.94 g (yield: 40.4%) of the intended product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06057330 |
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| Source dataset | uspto-grants-2000_05 |
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| ORD ID | ord-a72c5f83543e4b038a9194bee8e36eda |
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| Source note | uspto-grants-2000_05 |
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