HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1644829Generated: October 30, 2026
Isopropyl chloroformate → N-iso-propyloxycarbonyl-3-(4-imidazol-1-ylmethylphenyl)-5-iso-butylthiophene-2-sulfonamide
https://huagongshe.com/reaction/1644829
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isopropyl chloroformate | HCID 7917 | — |
| Reactant | 2-(Pyrrolidin-1-yl)pyridine | HCID 11019020 | — |
| Reactant | 3(4-Imidazol-1-ylmethylphenyl)5-iso-butylthiophene-2 sulfonamide | HCID 11394744 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | N-iso-propyloxycarbonyl-3-(4-imidazol-1-ylmethylphenyl)-5-iso-butylthiophene-2-sulfonamide | HCID 10161763 | 42.8% |
Reaction Steps
100 mg of crude 3-(4-imidazol-1-ylmethylphenyl)-5-iso-butylthiophene-2-sulfonamide (see Example 1(f) above) was dissolved in pyridine (4 mL, dried over 4 Å molecular sieve) and cooled on ice. Pyrrolidinopyridine (39.5 mg, 0.266 mmol) and iso-propyl chloroformate (1M in toluene, 2.66 mL, 2.66 mmol) were then added to the mixture. The mixture was stirred overnight under N2 atmosphere at 50° C. Evaporation and co-evaporation with acetonitrile to remove the solvents, followed by purification using preparative LC/MS (30% acetonitrile to pure acetonitrile, reverse phase) gave the title compound (52.6 mg, 0.114 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08124638B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-7e5e578b6067426d8a9e6d3662cf396b |
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| Source note | uspto-grants-2012_02 |
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