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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1969548Generated: November 2, 2026

Nordiazepam → Methyl 4-(cyclopropanesulfonamido)bicyclo[2.2.2]octane-1-carboxylate

https://huagongshe.com/reaction/1969548

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNordiazepamHCID 2997—
ReactantCyclopropanesulfonyl chlorideHCID 2760919—
ReactantMethyl 4-aminobicyclo[2.2.2]octane-1-carboxylateHCID 53426661—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductMethyl 4-(cyclopropanesulfonamido)bicyclo[2.2.2]octane-1-carboxylateHCID 5855723852.3%

Reaction Steps

To a solution of methyl 4-aminobicyclo[2.2.2]octane-1-carboxylate (500 mg, 2.73 mmol) (Yeh, V. S. C.; Kurukulasuriya, R.; Madar, D.; Patel, J. R.; Fung, S.; Monzon, K.; Chiou, W.; Wang, J.; Jacobson, P.; Sham, H. L.; Link, J. T. Bioorg. and Med. Chem. Let, 2006, vol. 16, #20 p. 5408-5413) in DCM (10 mL) at rt was added TEA (0.76 mL, 5.46 mmol) and DMAP (50 mg, 0.41 mmol). Cyclopropanesulfonyl chloride (764 mg, 5.46 mmol, Matrix) was added dropwise by syringe. The reaction mixture was stirred for about 15 h at rt. The mixture was washed with water (10 mL), and the aqueous layer was extracted with DCM (2×10 mL), the organic layers were combined and dried over anhydrous Na2SO4, filtered and concd in vacuo. The crude materials was purified by silica gel chromatography eluting with a gradient of 20-35% EtOAc in hexanes to afford methyl 4-(cyclopropanesulfonamido)bicyclo[2.2.2]octane-1-carboxylate (410 mg, 52% yield). LC/MS (Table 1, Method p) Rt=1.68 min; MS m/z: 288 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426411B2
Source datasetuspto-grants-2013_04
ORD IDord-108472bee9c84adeb0eb5189b9eb138b
Source noteuspto-grants-2013_04