HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12118Generated: October 30, 2026
Dichloromethane → HCID 11703849, compound
https://huagongshe.com/reaction/12118
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | HCID 22063467 | HCID 22063467 | — |
| Reactant | HCID 22063474 | HCID 22063474 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 11703849 | HCID 11703849 | — |
Reaction Steps
357 mg (1 mmol) of 6-benzyloxy-8-(2-ethoxy-2-hydroxy-acetyl)-4H-benzo[1,4]oxazin-3-one and 185 mg (1 mmol) of 2-(3,4-difluorophenyl)-1,1-dimethylethylamine are stirred for 30 minutes in 5 mL tetrahydrofuran at ambient temperature. It is cooled to 0° C. and, under an argon atmosphere, 1.5 mL of a 2 molar solution of lithium borohydride in tetrahydrofuran is added dropwise. The mixture is stirred for 30 minutes at ambient temperature, combined with 10 mL dichloromethane, and 3 mL water, stirred for a further hour and then filtered through an EXTRELUT® column. The eluate containing the ethanol amine is freed from solvent. The residue is dissolved in methanol and hydrogenated with palladium on charcoal (10%) as catalyst at 2.5 bar and ambient temperature. Then the catalyst is separated off and the crude product is purified by chromatography. White solid. Yield: 31 mg (6%, trifluoroethyl acetate); mass spectroscopy: [M+H]+=393.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07727984B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-4441e79696ac40c1bf0f8abad85e67ee |
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| Source note | uspto-grants-2010_06 |
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