HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2119028Generated: October 26, 2026
Methyl Anthranilate → HCID 178497648, compound
https://huagongshe.com/reaction/2119028
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl Anthranilate | HCID 8635 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | HCID 178479474 | HCID 178479474 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178497648 | HCID 178497648 | 77.5% |
Reaction Steps
Trans-4-guanidinomethylcyclohexanecarboxylic acid hydrochloride (111 g, 0.5 mole) (which is prepared by the method as disclosed in Japanese Patent First Publication No. 19694/1977, C.A., 87, 53269x) and methyl anthranilate (75.6 g, 0.5 mole) are dissolved in a mixture of dimethylformamide and pyridine (1:1, 1250 ml), and thereto is added dicyclohexylcarbodiimide (103 g, 0.5 mole), and the mixture is stirred at room temperature for 40 hours. After the undissolved materials are filtered off, the solvent is evaporated under reduced pressure. To the residue are added methanol (500 ml) and water (80 ml), and the mixture is stirred, and the undissolved materials are again filtered off and the solvent is evaporated under reduced pressure. The resulting residue is washed with acetone (2000 ml) and recrystallized from water to give the title compound (143 g) as white crystals. The physical data of this compound are identical with those of N-(o-methoxycarbonylphenyl)-trans-4-guanidinomethylcyclohexanecarboxamide hydrochloride prepared in Example 2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04681895 |
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| Source dataset | uspto-grants-1987_07 |
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| ORD ID | ord-f2f28c7b4cfd44d38ede490c8a516dcf |
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| Source note | uspto-grants-1987_07 |
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