HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2286621Generated: October 29, 2026
4-Methylmorpholine → HCID 178474779, compound
https://huagongshe.com/reaction/2286621
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | N2-Acetyl-L-glutamine | HCID 182230 | — |
| Reactant | HCID 178507442 | HCID 178507442 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178474779 | HCID 178474779 | 86.2% |
Reaction Steps
A solution of 14.1 g (75mmol) of N-acetyl-L-glutamine and 9.75 ml (75 mmol) of triethylamine in 150 ml of dimethylformamide is stirred at -15° to -20° C. and 9.75 ml (75 mmol) of isobutyl chloroformate is added. After stirring at -15° to -20° C. for 30 min a cold solution of 11.6 g (50 mmol) of 2-(4-aminophenyl)-4-hydroxy-5-pyrimidine carboxylic acid and 7.15 ml (50 mmol) of N-methylmorpholine in 200 ml of dimethylformamide is added at -15° C. The reaction mixture is stirred at -15° C. for 20 min at 5° C. for 3 hrs, and at room temperature overnight. The reaction mixture is evaporated and the residue treated with water. The pH is lowered to 2.5 with hydrochloric acid and the solid is filtered, washed with water, and dried to afford 17.3 g of 2-[4-(N-acetyl-DL-glutaminylamino)phenyl]-4-hydroxy-5-pyrimidine carboxylic acid; mp 247°-248° C. dec. [α]D25 -2.8 (c0.7, DMSO).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04267180 |
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| Source dataset | uspto-grants-1981_05 |
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| ORD ID | ord-e0ec169cc2994278b4ffcf9e68010d7f |
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| Source note | uspto-grants-1981_05 |
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