HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 647860Generated: October 30, 2026
2,3-Dihydroxybutanedioic Acid → 3-(S)-amino-1-ethoxycarbonylmethyl-2,3,4,5-tetrahydro-1H-[1]benzazepin-2-one tartrate salt
https://huagongshe.com/reaction/647860
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,3-Dihydroxybutanedioic Acid | HCID 875 | — |
| Reactant | 3-amino-1-ethoxycarbonylmethyl-2,3,4,5-tetrahydro-1H-[1]benzazepin-2-one | HCID 13243525 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(S)-amino-1-ethoxycarbonylmethyl-2,3,4,5-tetrahydro-1H-[1]benzazepin-2-one tartrate salt | HCID 22824509 | — |
Reaction Steps
Tartaric acid (12.6 g) and racemic 3-amino-1-ethoxycarbonylmethyl-2,3,4,5-tetrahydro-1H-[1]benzazepin-2-one (22 g) were dissolved in hot ethanol (200 ml). This solution was cooled and allowed to stand overnight at room temperature. The solid which precepitated was collected by filtration and recrystallized twice from ethanol (200 ml) to give 3-(S)-amino-1-ethoxycarbonylmethyl-2,3,4,5-tetrahydro-1H-[1]benzazepin-2-one tartrate salt. This was dissolved in H2O (100 ml) and the pH adjusted to 9 with dilute ammonium hydroxide and extracted with methylene chloride (2×50 ml). The combined extracts were washed with water (75 ml), dried (magnesium sulfate) and evaporated to give 3-(S)-amino-1-ethoxycarbonylmethyl-2,3,4,5-tetrahydro-1H-[1]benzazepin-2-one, m.p. 104°-106°, [α]D =-285.5° (c=0.99 in ethanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04410520 |
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| Source dataset | uspto-grants-1983_10 |
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| ORD ID | ord-247a4b9e4a7d4acf9b4be2334b671c5e |
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| Source note | uspto-grants-1983_10 |
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