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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDiazomethaneHCID 9550—
ReactantIsobutyl chloroformateHCID 62365—
Reactant2-(4-chloro-N-(pent-1-yn-3-yl)phenylsulfonamido)-butanoic acidHCID 59342373—
SolventAcetic AcidHCID 176—
SolventDiethyl EtherHCID 3283—
Product4-chloro-N-(1-diazo-2-oxopentan-3-yl)-N-(pent-1-yn-3-yl)benzenesulfonamideHCID 72259587—

Reaction Conditions

Temperature-30 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07732609B2
Source datasetuspto-grants-2010_06
ORD IDord-c6a04bb7504c4ce18d8cc8e65ca5dd39
Source noteuspto-grants-2010_06