HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972744Generated: November 1, 2026
Sodium borohydride → HCID 58529678, compound
https://huagongshe.com/reaction/1972744
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 58529850 | HCID 58529850 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 58529678 | HCID 58529678 | 74% |
Reaction Steps
To a solution of tert-butyl 3-[(4-aminopyrrolo[2,1-f][1,2,4]triazin-7-yl)carbonyl]azetidine-1-carboxylate (1.35 g, 4.25 mmol) in EtOH (25 mL) was added sodium borohydride (644 mg, 17.01 mmol). The mixture was stirred at 78° C. for 2 h. The reaction was quenched with the addition of H2O (20 mL). The resulting solid was removed by filtration and the filtrate was extracted with EtOAc (3×20 mL). The combined organics were washed with brine, dried (Na2SO4), and concentrated to dryness to afford 1.0 g (74%) of the desired product. ES-MS m/z 320.16 [M+H]+, HPLC RT (min) 2.02.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08431695B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-25f3fe2affc748488aa730afb56239df |
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| Source note | uspto-grants-2013_04 |
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