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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 644145Generated: October 29, 2026

Ethanol hydrochloride → HCID 86625849, compound

https://huagongshe.com/reaction/644145

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanol hydrochlorideHCID 21887872—
ReactantHCID 86625847HCID 86625847—
SolventEthanolHCID 702—
ProductHCID 86625849HCID 8662584976.5%

Reaction Steps

To an ethanol (5 mL) solution of 0.20 g of 4-(3-{4-[3-(4-{amino[(2S,3S)-2-(tert-butoxycarbonyl)amino-3-methylpentanoyloxyimino]methyl}phenoxy)propyl]-1-piperidinyl}propoxy)benzamide=O-[(2S,3S)-2 (tert-butoxycarbonyl)amino-3-methylpentanoyl]oxime was added 2 mL of 2.9 mol/L hydrogen chloride/ethanol at room temperature, which was then stirred at the same temperature for 5 hours. Thereto was added 2 mL of 2.9 mol/L hydrogen chloride/ethanol, which was then stirred for 26 hours. Thereto was further added 1 mL of 2.9 mol/L hydrogen chloride/ethanol, which was then stirred for 3 days. The solvent was distilled off under reduced pressure, and the resultant solid was suspended in diisopropyl ether, followed by collecting the solid matter by filtration before washing with diisopropyl ether to provide 0.13 g of 4-{3-[4-(3-{4-[amino((2S,3S)-2-amino-3-methylpentanoyloxyimino)methyl]phenoxy}propyl)-1-piperidinyl]propoxy}benzamide=O-((2S,3S)-2-amino-3-methylpentanoyl)oxime hydrochloride as white solid form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700623B2
Source datasetuspto-grants-2010_04
ORD IDord-d88ad4b901524b7689613579682aa234
Source noteuspto-grants-2010_04