HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1514210Generated: November 4, 2026
1,2-Dichloroethane → HCID 59403492, compound
https://huagongshe.com/reaction/1514210
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 2-(Trifluoromethyl)-[1,1'-biphenyl]-4-carboxylic acid | HCID 46315191 | — |
| Reactant | HCID 178451593 | HCID 178451593 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 59403492 | HCID 59403492 | 64.5% |
Reaction Steps
2-(Trifluoromethyl)-4-biphenylcarboxylic acid (Preparation 40) (284 mg, 1.07 mmol), HOBT (159 mg, 1.18 mmol) and EDC (225 mg, 1.18 mmol) were stirred in DMF (10 ml) under argon for 20 minutes. 1,1-Dimethylethyl 7-[(hydroxyamino)(imino)methyl]-1,2,4,5-tetrahydro-3H-3-benzazepine-3-carboxylate (Preparation 41) (326 mg, 1.07 mmol) was added and the mixture stirred at room temperature for 2.5 h before it was heated to 80° C. for 16 h. The reaction mixture was partitioned between EtOAc (30 ml) and water (30 ml) and the organic layer washed with aqueous sodium bicarbonate and water before it was dried (phase separator) and evaporated. The residue was triturated with methanol to give the title compound as a white solid (370 mg, 0.69 mmol). The filtrate was purified by Biotage Horizon, reverse phase cartridge, eluting with 5-100% acetonitrile in water to give further title compound (70 mg, 0.13 mmol). δH (d6DMSO, 400 MHz): 8.52 (1H, s), 8.50 (1H, d), 7.93 (1H, s), 7.90 (1H, dd), 7.74 (1H, d) 7.56-7.48 (3H, m), 7.41-7.38 (3H, m), 3.55-3.47 (4H, m), 3.02-2.93 (4H, m), 1.41 (9H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08222245B2 |
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| Source dataset | uspto-grants-2012_07 |
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| ORD ID | ord-8456e963a2474bbba1f11517fd4b77ab |
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| Source note | uspto-grants-2012_07 |
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