Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113733Generated: October 29, 2026

Pentane → 5-Diallylaminomethyl-thiophene-2-sulfonyl chloride

https://huagongshe.com/reaction/2113733

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPentaneHCID 8003—
ReactantChlorosuccinimideHCID 31398—
ReactantN-[(5-{[2-(4-{[3-chloro-5-(trifluoromethyl)pyridin-2-yl]amino}butanoyl)hydrazino]sulfonyl}thien-2-yl)methyl]-4-nitrobenzamideHCID 9895318—
ReactantHCID 178418306HCID 178418306—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product5-Diallylaminomethyl-thiophene-2-sulfonyl chlorideHCID 1138076953%

Reaction Conditions

Temperature-70 °C

Reaction Steps

A solution of the allyl-protected thiophene 19a (6.2 g, 32.1 mmol) in Et2O was cooled to −70° C. by means of an acetone/dry ice bath. A solution of t-BuLi in pentane (21.38 ml, 1.5M, 32.1 mmol) was added over 2 min whereupon the internal temperature momentarily rose to −50° C. and the mixture turned orange. After 10 min., SO2 was bubbled for 2 min, which led to the immediate formation of a thick precipitate. The reaction was allowed to reach 0° C., and a suspension of NCS (4.63 g, 32.1 mmol) in THF (20 ml) was added, whereupon the slurry turned purple. After 45 min at r.t., the mixture was filtered over SiO2, eluting with EtOAc. Evaporation, dilution with EtOAc:hexane 1:5 and filtration over SiO2 gave 5.0 g (53%) of the title sulfonyl chloride 19b as a pale brown oil which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07432286B1
Source datasetuspto-grants-2008_10
ORD IDord-0a46cfb1cc904262b085e15aa3a734f5
Source noteuspto-grants-2008_10