HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1395811Generated: November 4, 2026
4-Methylmorpholine → HCID 178501376, compound
https://huagongshe.com/reaction/1395811
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | Valyltyrosine methyl ester hydrochloride | HCID 14445713 | — |
| Reactant | HCID 178454196 | HCID 178454196 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178501376 | HCID 178501376 | — |
Reaction Steps
21.5 g of t-butoxycarbonylnitroarginine is dissolved in 200 ml of methylene chloride. 15.0 ml of N-methylmorpholine is added to the solution. The solution is cooled to -70° C. 8.8 ml of isobutyl chloroformate is then added. The reaction mixture is warmed up to -15° C. and stirred for 5 minutes. The reaction mixture is again cooled to -70° C. 22.3 g of valyltyrosine methyl ester hydrochloride is added to the reaction mixture. The reaction mixture is allowed to warm to room temperature, and then is stirred for 16 hours. The reaction mixture is extracted three times with 0.5 M potassium bisulfate and once with brine. The methylene chloride solution is dried over anhydrous sodium sulfate, filtered and stripped of solvent. The residue is dissolved in 200 ml of ethyl ether. The ether solution is added to cold rapidly stirring Skellysolve B. The white precipitate is filtered and dried to afford the product t-butoxycarbonylnitroarginylvalyltyrosine methyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04204991 |
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| Source dataset | uspto-grants-1980_05 |
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| ORD ID | ord-d78dbb0668664858aefc855b83fa47c9 |
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| Source note | uspto-grants-1980_05 |
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