HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 726708Generated: October 31, 2026
Lithium hydroxide, monohydrate → [(Z)-1-[4-(2-Biphenylylcarbonylamino)benzoyl]-4,4-difluoro-2,3,4,5-tetrahydro-1H-1-benzazepine-5-ylidene]acetic acid
https://huagongshe.com/reaction/726708
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium hydroxide, monohydrate | HCID 168937 | — |
| Reactant | [(Z)-1-[4-(2-Biphenylylcarbonylamino)benzoyl]-4,4-difluoro-2,3,4,5-tetrahydro-1H-1-benzazepine-5-ylidene]acetic acid methyl ester | HCID 10602784 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | [(Z)-1-[4-(2-Biphenylylcarbonylamino)benzoyl]-4,4-difluoro-2,3,4,5-tetrahydro-1H-1-benzazepine-5-ylidene]acetic acid | HCID 10554393 | 75.8% |
Reaction Steps
Methyl (Z)-[4,4-difluoro-1-[4-(2phenylbenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-1-benzazepin-5-ylidene]acetate (857 mg) was dissolved in 10 ml of methanol, 2 ml of aqueous solution containing 195 mg of lithium hydroxide monohydrate was added dropwise to the above solution under ice-cooling, and the mixture was stirred at room temperature for 7 hours. After evaporating the solvent under a reduced pressure, 1N hydrochloric acid aqueous solution was added, and the mixture was extracted with chloroform and dried over anhydrous magnesium sulfate. After evaporation of the solvent under a reduced pressure, the resulting residue was recrystallized from ethyl acetatehexane to obtain 633 mg of (Z)-[4,4-difluoro-1-[4-(2-phenylbenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-1-benzazepin-5-ylidene]acetic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05710150 |
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| Source dataset | uspto-grants-1998_01 |
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| ORD ID | ord-0ac6d333e3e14c50b4391bf4f72bbef0 |
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| Source note | uspto-grants-1998_01 |
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