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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 879470Generated: October 30, 2026

Methyl iodide → HCID 86700284, compound

https://huagongshe.com/reaction/879470

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 86700285HCID 86700285—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 86700284HCID 86700284—

Reaction Steps

To a solution of (S)-ethyl 2-tert-butoxy-2-(7-(4-chlorophenyl)-5-methyl-2-(1-oxoisoindolin-5-yl)benzo[d]thiazol-6-yl)acetate (94 mg, 0.171 mmol) in DMF (2.0 mL) was added NaH (˜10 mg, 60% oil dispersion) at 0° C. After 15 min, iodomethane (0.016 mL, 0.256 mmol) was added and after 30 min the reaction was allowed to warm to room temperature. Satd. aqueous NH4Cl was added and the reaction was diluted with EtOAc, washed sequentially with 5% aqueous LiCl and brine. The organic layer was dried over Na2SO4, concentrated and purified by flash column chromatography on silica gel using EtOAc to provide the title compound. LCMS-ESI+: calc'd for C31H31ClN2O4S: 563.2 (M+H+); found: 563.2 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987250B2
Source datasetuspto-grants-2015_03
ORD IDord-59d16eea51e44664a0957755748cb068
Source noteuspto-grants-2015_03