HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507079Generated: November 2, 2026
Phosphorus oxide (P4O10) → (+/-)-isopropyl 5-[(3,5-bistrifluoromethyl-benzyl)-(5-methyl-1H-pyrazol-3-yl)-amino)-8-chloro-2,3,4,5-tetrahydrobenzo[b]azepine-1-carboxylate
https://huagongshe.com/reaction/507079
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus oxide (P4O10) | HCID 14812 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | (+/-)-5-[(3,5-Bistrifluoromethyl-benzyl)-(3-oxo-butyryl)-amino]-8-chloro-2,3,4,5-tetrahydrobenzo[b]azepine-1-carboxylic acid isopropyl ester | HCID 59432322 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (+/-)-isopropyl 5-[(3,5-bistrifluoromethyl-benzyl)-(5-methyl-1H-pyrazol-3-yl)-amino)-8-chloro-2,3,4,5-tetrahydrobenzo[b]azepine-1-carboxylate | HCID 11585133 | 21.2% |
Reaction Steps
Add cold (ice bath) absolute EtOH (1 mL) slowly to a cooled 0° C. stirred mixture of (+/−)-5-[(3,5-bistrifluoromethyl-benzyl)-(3-oxo-butyryl)-amino]-8-chloro-2,3,4,5-tetrahydrobenzo[b]azepine-1-carboxylic acid isopropyl ester (118 mg, 0.20 mmol) and phosphorus pentoxide (511 mg, 3.6 mmol). Then, add hydrazine hydrate (0.062 mL, 2.0 mmol) dropwise while keeping the mixture cooled at 0° C. Heat at 100° C. overnight in a sealed tube. Cool down the mixture and remove the solvents under reduce pressure. Partition the residue between water and dichloromethane. Separate the layers, and dry organic phase over anhydrous magnesium sulfate, filter and concentrate in vacuo. Purify the residue by flash chromatography, eluting with hexanes/ethyl acetate, and then by a SCX cartridge to afford the title compound (25 mg, 21%). MS (ES+): 589 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07786108B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-81ff922805f84b1c9f9622e75eeeb76f |
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| Source note | uspto-grants-2010_08 |
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