HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1786653Generated: October 30, 2026
Hydrochloric Acid → HCID 178434315, compound
https://huagongshe.com/reaction/1786653
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Carbonic acid 2,5-dioxo-pyrrolidin-1-yl ester hexahydro-furo[2,3-b]furan-3-yl ester | HCID 17981482 | — |
| Reactant | HCID 178434316 | HCID 178434316 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 178434315 | HCID 178434315 | — |
Reaction Steps
{1-Benzyl-2-hydroxy-3-[isobutyl-(3-methyl-1H-indazole-5-sulfonyl)-amino]-propyl}-carbamic acid tert-butyl ester (25 mg, 0.047 mmol) was added to a solution of 4N HCl in dioxane (0.25 mL). Material precipitated out so 800 uL conc. HCl was added and the reaction heated at reflux for 2 h. The resulting solution was concentrated under vacuum and concentrated 2 additional times from 1 mL methylene chloride. This crude amine was dissolved in 0.5 mL methylene chloride and diisopropylethylamine (80 uL, 0.46 mmol) was then added. To this solution was added carbonic acid 2,5-dioxo-pyrrolidin-1-yl ester hexahydro-furo[2,3-b]furan-3-yl ester (16 mg, 0.055 mmol) and the reaction stirred overnight. The reaction was concentrated under vacuum and purified by preparative HPLC. MS 587 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07507763B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-ce026a901f9f47dc966a3a7150cbc0c2 |
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| Source note | uspto-grants-2009_03 |
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