HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 528865Generated: October 25, 2026
1,2-Dichloroethane → N3-(2-Aminobenzyl)-4-(4-chloro-3-(dibutylcarbamoyl)-5-methyl-1H-pyrazol-1-yl)-N1-(naphthalen-2-ylsulfonyl)isophthalamide
https://huagongshe.com/reaction/528865
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | 2-(Aminomethyl)aniline | HCID 178096 | — |
| Reactant | HOAt | HCID 181649 | — |
| Reactant | 2-(4-Chloro-3-(dibutylcarbamoyl)-5-methyl-1H-pyrazol-1-yl)-5-(naphthalen-2-ylsulfonylcarbamoyl)benzoic acid | HCID 71062145 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N3-(2-Aminobenzyl)-4-(4-chloro-3-(dibutylcarbamoyl)-5-methyl-1H-pyrazol-1-yl)-N1-(naphthalen-2-ylsulfonyl)isophthalamide | HCID 86718893 | 60% |
Reaction Steps
To a solution of 2-(4-chloro-3-(dibutylcarbamoyl)-5-methyl-1H-pyrazol-1-yl)-5-(naphthalen-2-ylsulfonylcarbamoyl)benzoic acid (Intermediate 91F, 50 mg, 0.080 mmol) in CH2Cl2 (1.1 mL) and DMF (0.2 mL) was added 2-(aminomethyl)aniline (20 mg, 0.16 mmol) followed by EDC (34 mg, 0.18 mmol) and 1-hydroxy-7-azabenzo-triazole (290 μL, 0.18 mmol, 0.6M solution in DMF). The resulting reaction mixture was stirred at room temperature overnight, then quenched with sat. aq. NH4Cl solution and extracted with EtOAc (3×). The combined organic extracts were dried over Na2SO4, filtered and concentrated in vacuo. Purification by flash column chromatography (gradient from 0% to 10% MeOH/CH2Cl2) provided the title compound (35 mg, 60%) as a pale yellow, oily solid. MS(ESI+) m/z 729.2 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09346795B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-b85120b236384e1394d1805b4b2fdfe9 |
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| Source note | uspto-grants-2016_05 |
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