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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1818764Generated: November 1, 2026

1-(Methoxymethyl)cyclopropane-1-sulfonamide → N-Propyl-1-sulfamoylcyclopropane-1-carboxamide

https://huagongshe.com/reaction/1818764

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Methoxymethyl)cyclopropane-1-sulfonamideHCID 22499277—
Reactant1-Propylcarbamoylcyclopropanesulfonamide tert-butylcarbamateHCID 66753294—
ProductN-Propyl-1-sulfamoylcyclopropane-1-carboxamideHCID 2249934850%

Reaction Steps

This compound was obtained in an optimized 50% yield from 1-propylcarbamoylcyclopropanesulfonamide tert-butylcarbamate (from Step B.3.a) according to the procedure described for the synthesis of 1-methoxymethylcyclopropylsulfonamide (Step B.1.b), except that no chromatography was used as the material was recrystallized from the minimum amount of CH2Cl2/hexanes: 1H NMR (CDCl3) δ 0.15 (m, 2H), 0.51 (m, 2H), 1.01 (m, 2H), 1.34 (m, 3H), 1.86 (d, J=7.0 Hz, 2H), 4.83 (s, 2H); 13C NMR (CDCl3) δ 4.65, 7.74, 11.26, 35.62, 41.21; LRMS m/z 193 (M++NH4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07601686B2
Source datasetuspto-grants-2009_10
ORD IDord-2c668ec6f28146e48a7d163df08803dc
Source noteuspto-grants-2009_10