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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1109536Generated: October 30, 2026

Methyl iodide → HCID 19020542, compound

https://huagongshe.com/reaction/1109536

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantHCID 14536608HCID 14536608—
SolventAcetoneHCID 180—
ProductHCID 19020542HCID 19020542—

Reaction Steps

A solution of N-(3-methylbutyl)-10-[1-(1-pyrolidinyl)-2-propyl]-2-phenothiazinecarboxamide, L series (1.5 g), and methyl iodide (0.94 cc) in acetone (50 cc) is stirred for 4 days at a temperature in the region of 20° C. The light yellow solution obtained is concentrated to dryness under reduced pressure (30 mm Hg; 4 kPa) at 40° C., and the light cream-colored meringue-like residue is suspended with stirring for 10 minutes in diethyl ether (100 cc), drained, washed with diethyl ether (2×10 cc) and dried at 40° C. under reduced pressure (5 mm Hg, 0.7 kPa). 1-Methyl-1-{2-[2-(3-methylbutyl)carbamoyl-10-phenothiazinyl]propyl}-pyrrolidinium iodide, L series (1.55 g) is thereby obtained in the form of a light beige powder, m.p. about 125°-130° C., the NMR spectrum of which is identical to that of the product of Example 11.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05321026
Source datasetuspto-grants-1994_06
ORD IDord-80d62a3c9a534c99adf6d1c33d23d2b2
Source noteuspto-grants-1994_06