HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 450724Generated: November 1, 2026
Hydrochloric Acid → HCID 178460133, compound
https://huagongshe.com/reaction/450724
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Propionylglycine | HCID 98681 | — |
| Reactant | HOAt | HCID 181649 | — |
| Reactant | HCID 67023917 | HCID 67023917 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178460133 | HCID 178460133 | 61% |
Reaction Steps
To a solution of N-(3,4-diamino-phenyl)-4-isopropyl-benzenesulfonamide×HCl (500 mg, 1.32 mmol) in DMF (20 ml) at 0° C. was added propionylamino-acetic acid (170 mg, 1.32 mmol) and 1-hydroxy-7-azabenzotriazole (HOAt) (220 mg, 1.59 mmol). After stirring the mixture at 0° C. for 15 min EDC (N-ethyl-N′-(3-dimethylaminopropyl)-carbodiimide) (300 mg, 1.45 mmol) was added. DIPEA (diisopropylethylamine) (0.92 ml, 5.29 mmol) was added after stirring another 15 min at 0° C. The mixture was stirred at room temperature for 16 h, and then concentrated under reduced pressure. The residue was partitioned between ethyl acetate and saturated aqueous NaHCO3 and the organic layer was dried over MgSO4, filtered, and the solvent evaporated under reduced pressure. A solution of the obtained oil in acetic acid was heated to 70° C. for 6 h. After evaporation of the solvent in vacuo the residue was purified by column chromatography to give the product as a yellow oil (320 mg, 61%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08486984B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-8d9ad607050c481cb04f0423e2542194 |
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| Source note | uspto-grants-2013_07 |
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