HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 904959Generated: October 30, 2026
Ethylmorpholine → HCID 131713280, compound
https://huagongshe.com/reaction/904959
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethylmorpholine | HCID 7525 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | N-Carbobenzoxy-L-valine | HCID 726987 | — |
| Reactant | Methyl O-tert-butyl-L-tyrosinate hydrochloride | HCID 6452451 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 131713280 | HCID 131713280 | — |
Reaction Steps
19.5 ml (approx. 150 mmoles) of N-ethylmorpholine and 33 g (160 mmoles) of DCC are added at 0° C. to a solution in 250 ml of dimethylformamide of 43.15 g (150 mmoles) of H-Tyr(But)-OMe.HCl, 37.65 g (150 mmoles) of Z-Val-OH and 20.25 g (150 mmoles) of 1-hydroxybenzotriazole. The mixture is stirred for 1 hour at 0° C. and is allowed to stand overnight at room temperature. The precipitate which has deposited is filtered off. It is rinsed with a little dimethylformamide. The filtrate is introduced into a mixture of 150 ml of saturated NaHCO3 solution and 3,000 ml of water, while stirring. The mixture is cooled to 4° C. and the precipitate is filtered off. It is washed thoroughly with water. While still wet, the product is dissolved in 400 ml of ethyl acetate. Insoluble matter is filtered off and water is separated off in a separating funnel. The ethyl acetate phase is dried over Na2SO4 and concentrated. The residue is triturated with petroleum ether and the product is filtered off. Yield 67 g (92%). Melting point 111°-112°, [α]D21 =-15.9° (c=1, methanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04420424 |
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| Source dataset | uspto-grants-1983_12 |
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| ORD ID | ord-6b5403b036bc4e2e92e7e0d7941fe6f2 |
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| Source note | uspto-grants-1983_12 |
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