HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175374Generated: October 29, 2026
Methane → Hexahydrofuro[2,3-b]furan-3-yl hydrogen {4-[(4-aminobenzene-1-sulfonyl)(2-methylpropyl)amino]-3-hydroxy-1-phenylbutan-2-yl}carbonimidate--ethanol (1/1)
https://huagongshe.com/reaction/2175374
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methane | HCID 297 | — |
| Reactant | Darunavir | HCID 213039 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Hexahydrofuro[2,3-b]furan-3-yl hydrogen {4-[(4-aminobenzene-1-sulfonyl)(2-methylpropyl)amino]-3-hydroxy-1-phenylbutan-2-yl}carbonimidate--ethanol (1/1) | HCID 23725083 | — |
Reaction Steps
100 gm of darunavir was dissolved in 1000 ml of denatured ethanol (mixture of 97% ethanol and 3% toluene) at 70-75° C. to obtain clear solution. 5 gm of activated charcoal was added and stirred for 120-150 minutes. The hot solution was filtered through hyflow bed and the bed was washed with 100 ml ethanol. The solution was filtered again through 0.2μ filter maintaining temperature at 70-75° C. The reaction mass was cooled to 15-20° C., stirred for an hour and filtered. The wet cake was washed with 100 ml of chilled ethanol and dried under vacuum at 40-45° C. to afford 89.5 gm of off white colored crystalline solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09062067B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-f6d748f3bc5245c8a6ab342d46058fb5 |
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| Source note | uspto-grants-2015_06 |
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