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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1456007Generated: November 1, 2026

Nitrogen → HCID 57250906, compound

https://huagongshe.com/reaction/1456007

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
Reactant2,6-LutidineHCID 7937—
ReactantTriisopropylsilyl trifluoromethanesulfonateHCID 2724529—
ReactantMethyl (3β)-3-hydroxy-7-oxochol-5-en-24-oateHCID 23250094—
SolventDichloromethaneHCID 6344—
ProductHCID 57250906HCID 5725090684.2%

Reaction Steps

To a solution of methyl 3β-hydroxy-7-oxochol-5-en-24-oate (2) (5.02 g, 12.5 mmoles) and 2,6-lutidine (3.32 ml, 28.5 mmoles) in CH2Cl2 (23 ml) cooled in an ice bath in a N2 atmosphere was added dropwise with magnetic stirring triisopropylsilyl trifluoromethanesulfonate (4.56 g, 17 mmoles). After 2 hrs, the reaction was diluted with CH2Cl2 (150 ml). It was then washed with cold 2N HCI, washed twice with H2O and then with saturated brine before drying with MgSO4. Evaporation in vacuo and purification of the residue by flash chromatography on silica gel with hexane-EtOAc (10:1) gave 5.88 g of 3 as a colorless syrup. NMR (CDCl3): δ 0.67 (s, 3H, 18-Me); 0.93 (d, 3H, 20-Me); 1.06 (s, 18H, TIPS Me); 1.19 (s, 3H, 19-Me); 3.66 (s, 3H, CO2Me); 3.68 (m, 1H, 3-H); 5.66 (s, 1H, 6-H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05843953
Source datasetuspto-grants-1998_12
ORD IDord-a51b04f147f54a7ea17556147262193a
Source noteuspto-grants-1998_12