HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(Bromomethyl)thiophene → 7-methoxy-naphthalene-2-sulfonic acid-[1-(2-cyanothiophene-4-ylmethyl)-2-oxopyrrolidin-3-(S)-yl]thiophene-3-ylmethylamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(Bromomethyl)thiophene | HCID 520703 | — |
| Reactant | HCID 10670821 | HCID 10670821 | — |
| Product | 7-methoxy-naphthalene-2-sulfonic acid-[1-(2-cyanothiophene-4-ylmethyl)-2-oxopyrrolidin-3-(S)-yl]thiophene-3-ylmethylamide | HCID 18392451 | — |
Reaction Steps
The title compound is prepared from 7-methoxynaphthalene-2-sulfonic acid [1-(2-cyanothiophen-4-ylmethyl)-2-oxopyrrolidin-3-(S)-yl]amide (0.5 g, 1.16 mmol) as described in EXAMPLE 126, Part A, using 3-bromomethylthiophene in place of methyl iodide. The crude product is purified by column chromatography eluting with 60% EtOAc/hexanes to afford 7-methoxy-naphthalene-2-sulfonic acid-[1-(2-cyanothiophene-4-ylmethyl)-2-oxopyrrolidin-3-(S)-yl]thiophene-3-ylmethylamide as a white solid (0.18 g, 0.33 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05958918 |
| Source dataset | uspto-grants-1999_09 |
| ORD ID | ord-576cd37cedc94e4f8cdf5d8c0616ada5 |
| Source note | uspto-grants-1999_09 |