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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 45257Generated: October 29, 2026

Methyl iodide → N-{(1R,3S)-3-[(benzyloxy)methyl]cyclopentyl}-6-chloro-N-methylpyridine-3-sulfonamide

https://huagongshe.com/reaction/45257

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantHCID 46701889HCID 46701889—
ReactantHCID 86659753HCID 86659753—
ProductN-{(1R,3S)-3-[(benzyloxy)methyl]cyclopentyl}-6-chloro-N-methylpyridine-3-sulfonamideHCID 8665975286%

Reaction Steps

According to process 23.2, starting with 0.66 g of 4 N-{(1R,3S)-3-[(benzyloxy)methyl]cyclopentyl}-6-chloropyridine-3-sulfonamide and 0.22 mL of methyl iodide, 0.58 g of N-{(1R,3S)-3-[(benzyloxy)methyl]cyclopentyl}-6-chloro-N-methylpyridine-3-sulfonamide is obtained in the form of an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541455B2
Source datasetuspto-grants-2013_09
ORD IDord-48a7993569234b09b01c2e162858ac2c
Source noteuspto-grants-2013_09