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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1192915Generated: November 1, 2026

Methyl iodide → HCID 66864972, compound

https://huagongshe.com/reaction/1192915

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantHCID 66864958HCID 66864958—
SolventDichloromethaneHCID 6344—
ProductHCID 66864972HCID 6686497277%

Reaction Steps

Ethyl 2-(1-methyl-3-(4-pentylphenylsulfonamido)azetidin-3-yl)acetate (10 mg, 0.026 mmol) was dissolved into CH2Cl2 (2 mL). The solution was treated with methyl iodide (37 mg, 0.26 mmol). The mixture was stirred at room temperature overnight. Solvent was removed under vacuum to obtain the title compound as a yellow solid (10 mg, 77%) which was used in the next step without purification. 1H NMR (400 MHz, CDCl3) δ 7.83 (d, 2H, J=8 Hz), 7.33 (d, 2H, J=8 Hz), 5.04 (m, 4H), 3.90 (q, 2H, J=7.2 Hz), 3.64 (s, 3H), 3.58 (m, 3H), 3.14 (s, 2H), 2.66 (t, 2H, J=8 Hz), 1.65-1.58 (m, 2H), 1.32 (br, 4H), 1.10 (t, 3H, J=7.2 Hz), 0.89 (m, 3H); MS ESI 397.2 [M]+, calcd for [C20H33N2O4S]+ 397.22.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680282B2
Source datasetuspto-grants-2014_03
ORD IDord-a3a73e912449499495a5a7a2c69414d3
Source noteuspto-grants-2014_03