HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1106114Generated: October 25, 2026
N-Acetyl-DL-methionine → HCID 178503723, compound
https://huagongshe.com/reaction/1106114
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Acetyl-DL-methionine | HCID 6180 | — |
| Reactant | Dimethylacetamide | HCID 31374 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | HCID 178507442 | HCID 178507442 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 178503723 | HCID 178503723 | 57.1% |
Reaction Steps
A suspension of 14.34 g (75 mmol) of N-acetyl-DL-methionine and 150 ml of dichloromethane is stirred at -15° and 10.5 ml (75 mmol) of triethylamine is added followed by 9.75 ml (75 mmol) of isobutyl chloroformate. After stirring for 20 minutes at -15° C., a solution of 11.6 g (50 mmol) of 2-(4-aminophenyl)-4-hydroxy-5-pyrimidine carboxylic acid in 200 ml of dimethylacetamide containing 7.7 ml (55 mmol) of triethylamine is added at -15° C. The mixture is stirred at 0° C. for 3 hrs and overnight at room temperature. The mixture is evaporated and the residue triturated with water. The aqueous suspension, after adjusting the pH to 2.5 with dilute HCl is filtered, washed with water, and dried to give 11.54 g of 2-[4-(N-acetyl-DL-methionylamino)phenyl]-4-hydroxy-5-pyrimidine carboxylic acid; mp 259° C. dec.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04311699 |
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| Source dataset | uspto-grants-1982_01 |
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| ORD ID | ord-05d69929a85042e98f25dfbd14c9cd8c |
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| Source note | uspto-grants-1982_01 |
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