HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 431519Generated: November 1, 2026
2-Mesitylenesulfonyl chloride → HCID 69637295, compound
https://huagongshe.com/reaction/431519
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Mesitylenesulfonyl chloride | HCID 13046 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 69637283 | HCID 69637283 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 69637295 | HCID 69637295 | 83.8% |
Reaction Steps
0.490 g (1.38 mmol) of (2S)-2-amino-3-((5-(2-methoxycarbonyl-ethyl)-thiophene-2-carbonyl)-amino)-propionic acid tert-butyl ester hydrochloride (example 15, step a) were dissolved in 15 ml of anhydrous dimethylformamide. Under stirring, 0.47 ml of N,N-diisopropyl-N-ethylamine and 0.302 g of 2,4,6-trimethylphenylsulfonyl chloride were added. Stirring was continued for 5 hours until the reaction was complete (thin layer chromatography). The solvents were removed in vacuo, and the residue was dissolved in ethyl acetate and washed with saturated sodium bicarbonate solution and with brine. After drying with anhydrous magnesium sulfate and filtration, the solvents were removed in vacuo to give 0.623 g of a yellow oil which was sufficiently pure for use in the subsequent step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06660728B2 |
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| Source dataset | uspto-grants-2003_12 |
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| ORD ID | ord-446a6c8957524fd6b72688b925f93482 |
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| Source note | uspto-grants-2003_12 |
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