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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1890515Generated: November 2, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → 2-(Azidomethyl)thieno[3,2-c]pyridine

https://huagongshe.com/reaction/1890515

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
ReactantThieno[3,2-c]pyridin-2-ylmethanolHCID 46784992—
SolventTetrahydrofuranHCID 8028—
Product2-(Azidomethyl)thieno[3,2-c]pyridineHCID 8667143088.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a flame-dried round-bottomed flask containing thieno[3,2-c]pyridin-2-ylmethanol (D-3) (3.2 g, 19.4 mmol) was added DPPA (8 g, 6.26 mL, 29.1 mmol) in THF (50 mL). The reaction mixture was stirred for 5 mins and cooled to 0° C., followed by adding DBU (4.43 g, 4 mL, 29.1 mmol) via syringe. The mixture was allowed to stir at reflux overnight. The reaction was then partitioned between water and ethyl ether. The aqueous layer was extracted with ethyl ether. The combined organic layers were washed with brine, dried over Na2SO4, concentrated, and purified by chromatography to afford the product (3.27 g). MS (m/z): 191 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507487B2
Source datasetuspto-grants-2013_08
ORD IDord-cbfa1ff6c8654ee987230a715104315a
Source noteuspto-grants-2013_08