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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234727Generated: October 31, 2026

Nitrogen → HCID 57250906, compound

https://huagongshe.com/reaction/234727

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
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 313-hydroxy-7-oxochol-5-en-24-oate (2) (5.02 g, 12.5 mmoles) and 2,6-1utidine (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 HCl, 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): δ0.67 (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 numberUS05595996
Source datasetuspto-grants-1997_01
ORD IDord-e79937d60d984ae6b527a3f8319d44e9
Source noteuspto-grants-1997_01