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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1969175Generated: October 31, 2026

Water → Tert-butyl (6-chloro-4-iodopyridin-3-yl)(methyl)carbamate

https://huagongshe.com/reaction/1969175

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactanttert-Butyl (6-chloro-4-iodopyridin-3-yl)carbamateHCID 53415320—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl (6-chloro-4-iodopyridin-3-yl)(methyl)carbamateHCID 5744339999.4%

Reaction Steps

To the solution of tert-butyl (6-chloro-4-iodopyridin-3-yl)carbamate (61 g, 0.172 mol) in 300 mL of anhydrous THF was added 60% NaH (7.6 g, 0.189 mol) at 0° C. under N2 atmosphere. After the addition was finished, the solution was stirred for 30 min, and then the solution of MeI (26.92 g, 0.189 mol) in 100 mL of dry THF was added. Then the solution was stirred at 0° C. for 3 hrs. TLC indicated the reaction was over. Water was added for quench, and EtOAc was added to extract twice. The combined organic phases were washed with brine, dried over Na2SO4, filtered and concentrated to afford 63 g of crude tert-butyl (6-chloro-4-iodopyridin-3-yl)(methyl)carbamate used into the following de-protection without the further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426450B1
Source datasetuspto-grants-2013_04
ORD IDord-15b000c8b7be4d4ca220ae1843198ca8
Source noteuspto-grants-2013_04