HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 899869Generated: October 25, 2026
1-Hydroxybenzotriazole → Methyl 2-{[(4-{2-[(2,4-difluorobenzyl)(heptyl)amino]-2-oxoethyl}phenyl)thio]methyl}benzoate
https://huagongshe.com/reaction/899869
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| Reactant | N-(2,4-difluorobenzyl)-N-heptylamine | HCID 60663854 | — |
| Reactant | (4-{[2-(Methoxycarbonyl)benzyl]thio}phenyl)acetic acid | HCID 69120445 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 2-{[(4-{2-[(2,4-difluorobenzyl)(heptyl)amino]-2-oxoethyl}phenyl)thio]methyl}benzoate | HCID 69120607 | 77.4% |
Reaction Steps
(4-{[2-(Methoxycarbonyl)benzyl]thio}phenyl)acetic acid (581 mg, 1.836 mmol) and N-(2,4-difluorobenzyl)-N-heptylamine (465.3 mg, 1.968 mmol) were combined in DMF and the mixture was cooled in an ice-bath. HOBT (260.6 mg, 1.928 mmol) and TBTU (619 mg, 1.928 mmol) were added, followed by DIPEA (747.7 mg 5.785 mmol). The mixture was stirred at room temperature overnight and then evaporated. The resulting mixture was partitioned between ethyl acetate and sodium hydrogencarbonate aqueous solution (sat.). The aqueous portion was extracted with ethyl acetate and the combined organic extracts was dried with magnesium sulphate and then evaporated. Chromatography of the residue on a column (ISOLUTE® SI, 20 g/70 ml) using ethyl acetate/heptane (5:95, then 10:90) as eluant gave 767 mg the desired product, yield 77%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07355069B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-86778b2ba32f4adf8e46b31abd75301b |
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| Source note | uspto-grants-2008_04 |
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