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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1669488Generated: October 30, 2026

Tetrahydrofuran → HCID 67343811, compound

https://huagongshe.com/reaction/1669488

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 67344360HCID 67344360—
ReactantHCID 178482962HCID 178482962—
SolventEthyl AcetateHCID 8857—
ProductHCID 67343811HCID 6734381158%

Reaction Conditions

Temperature40 °C

Reaction Steps

To a solution of methyl 14-cyclohexyl-7-(3-piperazin-1-ylpropyl)-7,8-dihydro-6H-indolo[1,2-e][1,5]benzoxazocine-11-carboxylate (0.11 M) in dry THF was added (tert-butoxycarbonyl){[4-(dimethyliminio)pyridin-1(4H)-yl]sulfonyl}azanide (1 eq) (prepared following literature procedure: Winum, J.-Y. et al Org. Lett. 2001, 3, 2241-2243) and the mixture stirred at 40° C. for 2 h. The reaction was allowed to cool to RT before diluting with EtOAc. The combined organics were washed with 1N HCl (aq), sat. aq. NaHCO3 then brine, dried (Na2SO4), filtered and concentrated in vacuo to afford the product as a yellow foam (58%) that was used without further purification. (ES+) m/z 695 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07989438B2
Source datasetuspto-grants-2011_08
ORD IDord-cfc53263109043a3aca365efd94759a3
Source noteuspto-grants-2011_08