HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1369554Generated: October 29, 2026
2-(2-Chloroethyl)-1-methylpyrrolidine → HCID 22291035, compound
https://huagongshe.com/reaction/1369554
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-(2-Chloroethyl)-1-methylpyrrolidine | HCID 285093 | — |
| Reactant | HCID 22291011 | HCID 22291011 | — |
| Product | HCID 22291035 | HCID 22291035 | — |
Reaction Steps
As described hereinbefore in Example 7, 2-(2-chloroethyl)-N-methylpyrrolidine was reacted with N-[2-methyl-5-(3-morpholinobenzamido)phenyl]-3-hydroxybenzamide and the reaction product was purified by column chromatography on silica using a 9:1 mixture of methylene chloride and methanol as eluent. There was thus obtained N-[2-methyl-5-(3-morpholinobenzamido)phenyl]-3-[2-(N-methylpyrrolidin-2-yl)ethoxy]benzamide (Example 7, Compound No. 32). On further elution an isomeric by-product was obtained. There was thus obtained the title compound NMR Spectrum: (DMSOd6) 1.6 (m, 1H), 1.79 (m, 3H), 2.04 (m, 2H), 2.17 (s, 3H), 2.24 (s, 3H), 2.52 (m, 4H), 3.18 (t, 4H), 3.76 (t, 4H), 4.66 (m, 1H), 7.1 (m, 2H), 7.21 (d, 1H), 7.4 (m, 4H), 7.5 (d, 1H), 7.56 (m, 1H), 7.78 (d, 1H), 9.83 (s, 1H), 10.11 (s, 1H); Mass Spectrum: M+H+543.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06579872B1 |
|---|
| Source dataset | uspto-grants-2003_06 |
|---|
| ORD ID | ord-6121f672cd2243b88b2ade4589dd1fa7 |
|---|
| Source note | uspto-grants-2003_06 |
|---|