HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 15727Generated: October 23, 2026
Triethylamine → 4-chloro-N-(1-diazo-2-oxopentan-3-yl)-N-(pent-1-yn-3-yl)benzenesulfonamide
https://huagongshe.com/en/reaction/15727
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Diazomethane | HCID 9550 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | 2-(4-chloro-N-(pent-1-yn-3-yl)phenylsulfonamido)-butanoic acid | HCID 59342373 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4-chloro-N-(1-diazo-2-oxopentan-3-yl)-N-(pent-1-yn-3-yl)benzenesulfonamide | HCID 72259587 | — |
Reaction Steps
To a solution of the compound 60 (498 mg, 1.45 mmol) in 7.5 mL of Et2O were added sequentially 0.24 mL of triethylamine (1.2 eq), 0.23 mL of isobutyl chloroformate (1.2 eq) at −30° C. After being stirred at −30° C. for 15 min, diazomethane (prepared by mixing MNNG and KOH in diethyl ether) (excess) was added to the above mixture at 0° C. and stirred there for 5 hours. Glacial HOAc (1.5 mL) was added to destroy the excess diazomethane and the solution was extracted with EtOAc. The organic phase was washed with sat NaHCO3, water, brine and dried (MgSO4). LCMS 368.1 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07732609B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-c6a04bb7504c4ce18d8cc8e65ca5dd39 |
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| Source note | uspto-grants-2010_06 |
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