HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016151Generated: October 29, 2026
1,2-Dichloroethane → HCID 57888900, compound
https://huagongshe.com/reaction/1016151
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 3-Sulfamoylbenzoic acid | HCID 229352 | — |
| Reactant | HCID 57889325 | HCID 57889325 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57888900 | HCID 57888900 | 70.7% |
Reaction Steps
(R)-2-Amino-1-((S)-4-(4-chlorophenyl)-4-hydroxy-3,3-dimethylpiperidin-1-yl)-3-methylbutan-1-one (200 mg, 0.533 mmol), 3-sulfamoylbenzoic acid (129 mg, 0.639 mmol), HOBT (98 mg, 0.639 mmol), EDC (123 mg, 0.639 mmol) and triethylamine (0.149 mL, 1.066 mmol) were mixed in methylene chloride (3 mL) at 25° C. with stirring. The reaction was stirred for 20 hours then washed with sat'd sodium bicarbonate. The methylene chloride layer was dried over sodium sulfate and concentrated in vacuo to give a white glass which was purified over silica gel (1:1 Hexanes/EtOAc to 100% EtOAc) to obtain N-((R)-1-((S)-4-(4-chlorophenyl)-4-hydroxy-3,3-dimethylpiperidin-1-yl)-3-methyl-1-oxobutan-2-yl)-3-sulfamoylbenzamide (197 mg, 0.377 mmol, 70% yield) as a white glass. MS found: (M+H)+=522.32.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07985861B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-56daa31f871d4033bcf19db84936270d |
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| Source note | uspto-grants-2011_07 |
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