Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 70002371 | HCID 70002371 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 18551832 | HCID 18551832 | 87.4% |
Reaction Steps
The (RS)-(4-carbamimidoyl-phenylamino)-[5-ethoxy-2-fluoro-4-(2-hydroxy-ethoxy)-phenyl]-acetic acid ethyl ester hydrochloride (172 mg) described in example 1.6 was suspended in THF (1.1 ml). A solution of NaOH (0.82 ml, 1 M in H2O) was added and stirred for 30 min at 0° C. and for 40 min at room temperature. 1M HCl (0.41 ml) was added. The mixture was concentrated. The solid was washed with water and ether and dried to give 129 mg of (RS)-(4-carbamimidoyl-phenylamino)-[5-ethoxy-2-fluoro-4-(2-hydroxy-ethoxy)-phenyl]-acetic acid as a colorless solid. MS: 392 ([M+H]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06548694B2 |
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| Source dataset | uspto-grants-2003_04 |
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| ORD ID | ord-973c00c271ea467b81c0c8820acbb877 |
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| Source note | uspto-grants-2003_04 |
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