HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 963043Generated: October 30, 2026
Hydrochloric Acid → HCID 67727688, compound
https://huagongshe.com/reaction/963043
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1H-indole-2-carbonyl Chloride | HCID 11816208 | — |
| Reactant | HCID 67727694 | HCID 67727694 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 67727688 | HCID 67727688 | 3.4% |
Reaction Steps
4-(2-Chlorophenyl)-9-(2-ethoxycarbonylethyl)-2-ethyl-6H-thieno[3,2-f] [1,2,4]triazolo[4,3-a] [1,4]diazepine (5.78 g) was heated with 5% hydrochloric acid for 3 hours, and the mixture was cooled to room temperature. Sodium hydrogencarbonate (25.2 g) and chloroform were added. Indole-2-carbonyl chloride (2.67 g) was added with vigorous stirring, and the mixture was stirred for 4 hours. The organic layer was concentrated, and the residue was dissolved in methanol (39 ml). The solution was hydrolyzed with 2M sodium hydroxide (3.9 ml) and the reaction mixture was made acidic. The mixture was extracted with ethyl acetate and the extract was dried over magnesium sulfate. The solvent was evaporated and the obtained residue was recrystallized from ethanol to give 0.26 g of 3-(4-(3-(2-chlorobenzoyl)-5-ethylthiophen-2-yl)-3-(indole-2-carbonylaminomethyl) [1,2,4]triazol-5-yl)propionic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05760032 |
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| Source dataset | uspto-grants-1998_06 |
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| ORD ID | ord-b3a7be489b814246abcb51bc9cc2fc21 |
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| Source note | uspto-grants-1998_06 |
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