HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108276Generated: October 30, 2026
O-methyl-L-tyrosine N-Methylamide → 6-Methyl-4-[[[1-[(methylamino)carbonyl]-2-(4-methoxyphenyl)ethyl]amino]carbonyl]hept-3-enoic acid, methyl ester
https://huagongshe.com/reaction/2108276
Participants
| Role | Name | HCID | Charge |
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| Reactant | O-methyl-L-tyrosine N-Methylamide | HCID 14303038 | — |
| Reactant | 4-Methoxycarbonyl-2-(2-methylpropyl)but-2-enoic acid | HCID 53859812 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-Methyl-4-[[[1-[(methylamino)carbonyl]-2-(4-methoxyphenyl)ethyl]amino]carbonyl]hept-3-enoic acid, methyl ester | HCID 85115234 | 53.3% |
Reaction Steps
N,N-Dicyclohexylcarbodiimide (515 mg, 2.5 mmol) was added to an ice-cooled solution of 4-methoxycarbonyl-2-(2-methylpropyl)but-2-enoic acid (500 mg, 2.5 mmol) and O-methyl-L-tyrosine N-methylamide (520 mg, 2.5 mmol) in dry dichloromethane (30 ml), and the mixture was stirred at room temperature for 18 h. The precipitated solid was filtered off and washed with a little dichloromethane, then the organic solution was washed successively with 1N hydrochloric acid (20 ml), 1N sodium bicarbonate (20 ml), and water. The solution was dried (MgSO4) and evaporated in vacuo. Column chromatography (30 g silica) of the residual solid, eluting with 5% methanol/dichloromethane gave the title compound (520 mg, 53%), m.p. 142°-144° C. (dichloromethane/pentane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04937243 |
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| Source dataset | uspto-grants-1990_06 |
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| ORD ID | ord-5df8e4a4564241689f6433ba7df44eee |
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| Source note | uspto-grants-1990_06 |
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