HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2373608Generated: October 29, 2026
Sodium borohydride → HCID 57444325, compound
https://huagongshe.com/reaction/2373608
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | N-(3-{2-[4-(2-methyl-5-quinolinyl)-1-piperazinyl]acetyl}phenyl)acetamide | HCID 57444326 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57444325 | HCID 57444325 | 42% |
Reaction Steps
Sodium borohydride (0.015 g, 1.6 eq) was added to a stirred solution of N-(3-{2-[4-(2-methyl-5-quinolinyl)-1-piperazinyl]acetyl}phenyl)acetamide (0.102 g, 1 eq) in dry DCM (2 mL) cooled to 0° C. under an inert atmosphere. The reaction was warmed to room temperature and stirred for 18 hours. The mixture was diluted with DCM (10 mL) and washed with water (2×10 mL). The organic phase was dried over sodium sulfate and the solvent was removed under reduced pressure. The crude material was purified on SPE cartridge (Silica) using as eluant DCM-methanol (97:3), affording the title compound in 42% yield (0.104 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07459456B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-2abe89e302444fb7a6cce5a4f8aa799e |
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| Source note | uspto-grants-2008_12 |
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