HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1927701Generated: October 30, 2026
Toluene → 2,4-bisbenzyloxy-N-butyl-5-(5-hydroxy-1,3-dihydroisoindole-2-carbonyl)-N-methylbenzamide
https://huagongshe.com/reaction/1927701
Participants
| Role | Name | HCID | Charge |
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| Reactant | Toluene | HCID 1140 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 5-[(N-Methyl-N-butylamino)carbonyl]-2,4-bisbenzyloxybenzoic acid | HCID 59614060 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,4-bisbenzyloxy-N-butyl-5-(5-hydroxy-1,3-dihydroisoindole-2-carbonyl)-N-methylbenzamide | HCID 59614094 | 54% |
Reaction Steps
652.9 μl (9 mmol) of thionyl chloride are added to a suspension of 2.06 g (4.6 mmol) of 2,4-bisbenzyloxy-5-[(N-methyl-N-butylamino) carbonyl]benzoic acid (5) in 20 ml of THF (dry), and the mixture is stirred for 15 min at 22° C. 10 ml of toluene are subsequently added, and the mixture is evaporated to dryness in vacuo at 40° C. The residue is dissolved in 20 ml of THF and added to a suspension of 800 mg (4.661 mmol) of 2,3-dihydro-1H-isoindol-5-ole hydrochloride in 30 ml of dichloromethane, 5 ml of THF and 1.7 ml (10 mmol) of N-ethyldiisopropylamine. After 2 h at 22° C., the mixture is evaporated and chromatographed over an RP18 column. Evaporation to dryness in vacuo gives 1.4 g (54%) of 2,4-bisbenzyloxy-N-butyl-5-(5-hydroxy-1,3-dihydroisoindole-2-carbonyl)-N-methylbenzamide as beige crystals, MW 564.7;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08183279B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-94a52d0c19b848808807054dc9e2cf74 |
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| Source note | uspto-grants-2012_05 |
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