HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2353862Generated: November 2, 2026
Sodium Hydroxide → 5-(3,5-Bis-trifluoromethyl-benzylamino)-2,3,4,5-tetrahydro-benzo[b]azepine-1-carboxylic acid isopropyl ester
https://huagongshe.com/reaction/2353862
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3,5-Bis(trifluoromethyl)benzylamine | HCID 521099 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Isopropyl 5-oxo-2,3,4,5-tetrahydro-1H-benzo[b]azepine-1-carboxylate | HCID 68680367 | — |
| Catalyst | Titanium isopropoxide | HCID 11026 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-(3,5-Bis-trifluoromethyl-benzylamino)-2,3,4,5-tetrahydro-benzo[b]azepine-1-carboxylic acid isopropyl ester | HCID 86616062 | — |
Reaction Steps
A mixture of 5-Oxo-2,3,4,5-tetrahydro-benzo[b]azepine-1-carboxylic acid isopropyl ester (283 mg, 1.14 mmol), 3,5-Bis(trifluoromethyl)benzylamine (304 mg, 1.25 mmol) and titanium(IV) isopropoxide (0.43 ml, 1.43 mmol) was stirred at room temperature for 6 hours. The mixture was diluted with methanol (5 ml) and treated with sodium borohydride (65 mg, 1.71 mmol), then stirred at room temperature for 18 hours. The mixture was treated with 0.1N NaOH (25 ml) and stirred for 10 minutes, then filtered through Celite. The filtered residue washed successively with diethyl ether and dichloromethane. The filtrate was transferred to a separatory funnel and the organic layer was separated, dried (Na2SO4) and concentrated to provide crude 5-(3,5-Bis-trifluoromethyl-benzylamino)-2,3,4,5-tetrahydro-benzo[b]azepine-1-carboxylic acid isopropyl ester, which was elaborated without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07749992B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-c5ee00e63ac8466fab8c7ec02f300f4b |
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| Source note | uspto-grants-2010_07 |
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