HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Chloro-2-nitroaniline → 5-(3-Methoxymethyl-pyrrol-1-yl)-2-nitro-phenylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Chloro-2-nitroaniline | HCID 74218 | — |
| Reactant | 2,5-Dimethoxy-3-methoxymethyl-tetrahydro-furan | HCID 18548706 | — |
| Reactant | N-(5-amino-2-nitro-phenyl)-acetamide | HCID 18548776 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 5-(3-Methoxymethyl-pyrrol-1-yl)-2-nitro-phenylamine | HCID 18548853 | — |
Reaction Steps
The title compound was prepared from N-(5-amino-2-nitro-phenyl)-acetamide [prepared from commercially available 5-chloro-2-nitroaniline as described in Example F6] and 2,5-dimethoxy-3-methoxymethyl-tetrahydro-furan [prepared from (2,5-dimethoxy-tetrahydro-furan-3-yl)-methanol [CAS-no. 207119-66-2] by methylation with 2.1 eq. NaH (95%) and 5.5 eq. Mel in Et2O at 0° C. for 2 h] in HOAc at 60° C. for 18 h according to the general procedure F. Obtained as a light yellow solid (86 mg). Deacetylation of this material was perfomed by stirring with 2 eq. 2 N NaOH-sol. in 1,4-dioxane at 60° C. for 2 h. Obtained as a yellow solid (69 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06548495B2 |
| Source dataset | uspto-grants-2003_04 |
| ORD ID | ord-a68e62bfa17f4fc1b5181ba23c34e550 |
| Source note | uspto-grants-2003_04 |