HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 732686Generated: October 29, 2026
1,4-Dioxane hydrochloride → HCID 68914533, compound
https://huagongshe.com/reaction/732686
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,4-Dioxane hydrochloride | HCID 20443148 | — |
| Reactant | HCID 86628551 | HCID 86628551 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 68914533 | HCID 68914533 | 70.6% |
Reaction Steps
A 1.6 ml 1,4-dioxane solution of 110 mg of tert-butyl ({(3R,4S)-1-[4-(aminosulfonyl)benzoyl]-4-phenylpyrrolidin-3-yl}methyl)[(1R)-1-(1-naphthyl)ethyl]carbamate was mixed with 1.5 ml of 4 M hydrogen chloride/1,4-dioxane and stirred at room temperature for 60Hours. The reaction solution was concentrated under a reduced pressure, mixed with water and neutralized with saturated sodium bicarbonate solution. The organic layer extracted with chloroform was dried with anhydrous sodium sulfate and then concentrated under a reduced pressure. By crystallizing the thus obtained residue from ethyl acetate, 65 mg of 4-{[(3S,4S)-3-({[(1R)-1-(1-naphthyl)ethyl]amino}methyl)-4-phenylpyrrolidin-1-yl]carbonyl}benzene sulfonamide was obtained as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07585886B2 |
|---|
| Source dataset | uspto-grants-2009_09 |
|---|
| ORD ID | ord-6d2b8a2b3ff648d3a987b0d236b47c11 |
|---|
| Source note | uspto-grants-2009_09 |
|---|