HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 985095Generated: October 30, 2026
Ammonium Chloride → HCID 10215337, compound
https://huagongshe.com/reaction/985095
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 69586067 | HCID 69586067 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 10215337 | HCID 10215337 | 78% |
Reaction Steps
6.0 g of (8R,9R)-8-hydroxy-2-methoxymethyl-3-methyl-9-phenyl-7,8,9,10-tetrahydro-imidazo[1,2-h][1,7]naphthyridin-7-one are suspended in 40 ml methanol and 0.6 g sodium borohydride are added in small portions over a period of 30 min. After 1 h at ambient temperature the reaction mixture is poured onto of 60 ml icewater and 2 g ammonium chloride. The organic layer is separated and the aqueous phase extracted three times with dichloromethane. The combined organic phases are dried over anhydrous sodium sulfate and the solvent removed in vacuo. The residue is purified by column chromatography on silica gel (eluent: dichloromethane/methanol 100:1). Crystallization from diethyl ether yields 4.7 g (78%) of the title compound as a light brown solid (BYK237362, m.p. 102-104° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06869949B2 |
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| Source dataset | uspto-grants-2005_03 |
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| ORD ID | ord-d4b57515bdaa4ebdad834c790a4f35d1 |
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| Source note | uspto-grants-2005_03 |
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