HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607415Generated: October 30, 2026
4-Methylmorpholine → HCID 178501400, compound
https://huagongshe.com/reaction/1607415
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Di(succinimido) carbonate | HCID 676246 | — |
| Reactant | HCID 57214422 | HCID 57214422 | — |
| Reactant | HCID 178419105 | HCID 178419105 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178501400 | HCID 178501400 | 73.8% |
Reaction Steps
A solution of 330 mg of 2-benzylidene-3-(1-naphthylmethylcarbamoyl)propionic acid, 260 mg of N,N'-disuccinimidylcarbonate and 1 ml of pyridine in 20 ml of dry acetonitrile was stirred for 3 hour at room temperature. The solution was added to a solution of 300 mg of L-histidine methyl ester dihydrochloride and 150 mg of N-methylmorpholine in 20 ml of dry N,N-dimethylformamide, and the mixture was stirred for 16 hours at 40° C. The reaction mixture was concentrated under reduced pressure, and a 5% aqueous sodium bicarbonate solution was added to the residue. The precipitates were collected by filtration to obtain 350 mg of N-[2-benzylidene-3-(1-naphthylmethylcarbamoyl)propionyl]-L-histidine methyl ester as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04863904 |
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| Source dataset | uspto-grants-1989_09 |
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| ORD ID | ord-31e9289029fe4c73b7d5836dcdb84c4c |
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| Source note | uspto-grants-1989_09 |
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