HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 718122Generated: October 29, 2026
Sodium Iodide → Methyl 4-(2-(2-aminoacetamido)thiophene-3-carbonyl)benzoate
https://huagongshe.com/reaction/718122
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Methyl 4-(2-aminothiophene-3-carbonyl)benzoate | HCID 59783735 | — |
| Reactant | dry ice acetone Ammonia | HCID 86707873 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 4-(2-(2-aminoacetamido)thiophene-3-carbonyl)benzoate | HCID 59783705 | 28% |
Reaction Steps
In a 100 mL round-bottomed flask was dissolved title compound 491 (1 g, 2.96 mmol) and sodium iodide (0.533 g, 3.55 mmol) in tetrahydrofuran (20 mL) to give a yellow suspension. The mixture was heated at reflux for 2 hours. The mixture was cooled to −78° C. A Dewar-type condenser was attached and filled with dry ice/acetone Ammonia was introduced as a gas and about 30 mL was condensed into the flask. The reaction mixture was left to warm up to room temperature over the weekend. The solvent was removed in vacuo and the residue was purified via ISCO (50-100% EtOAc/Hexanes; 40 g silica gel column) to obtain product as a tan powder. The solid was purified by suspending it in 1:1 dichloromethane/ether and filtering to afford title compound 492 (265 mg, 28%) as a tan powder which was sufficiently pure for the next step. MS (m/z): 319.3 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09193749B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-d2acebff371249f1b2b53f26ef2aa78d |
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| Source note | uspto-grants-2015_11 |
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