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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2119028Generated: October 26, 2026

Methyl Anthranilate → HCID 178497648, compound

https://huagongshe.com/reaction/2119028

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl AnthranilateHCID 8635—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantHCID 178479474HCID 178479474—
SolventPyridineHCID 1049—
SolventDimethylformamideHCID 6228—
ProductHCID 178497648HCID 17849764877.5%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04681895
Source datasetuspto-grants-1987_07
ORD IDord-f2f28c7b4cfd44d38ede490c8a516dcf
Source noteuspto-grants-1987_07