HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1746834Generated: October 31, 2026
Benzenesulfonamide → HCID 71179013, compound
https://huagongshe.com/reaction/1746834
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzenesulfonamide | HCID 7370 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | L-Glutamic acid, N-((1,1-dimethylethoxy)carbonyl)-, 5-(phenylmethyl) ester | HCID 83589 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 71179013 | HCID 71179013 | — |
Reaction Steps
1.7 g (5.0 mmol) of Boc-Glu (OBzl)-OH, 1.03 g (5.0 mmol) of dicyclohexylcarbodiimide and 611 mg (5.0 mmol) of 4-(dimethylamino)pyridine were suspended in 20 ml of methylene chloride, to which 866 mg (5.0 mmol) of benzenesulfonamide was added. Following agitation at room temperature overnight, extraction was performed with ethyl acetate/1N hydrochloric acid. The organic layer was washed with saturated saline and then added with sodium sulfate for drying. The organic layer was subjected to vacuum condensation. To the resulting residue, 100 mg of 10% Pd/C and 20 ml of methanol were added and stirred overnight in a hydrogen atmosphere under a normal pressure. After filtrating the catalyst away, the solvent was distilled away and purification step A was used to obtain a crude product of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09150505B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-f7b0b4c88db4403cb69b5d50aff1feab |
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| Source note | uspto-grants-2015_10 |
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