HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-methoxy-N-methyl-4-nitrobenzamide → (1-Methyl-1H-imidazol-5-yl)(4-nitrophenyl)methanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-methoxy-N-methyl-4-nitrobenzamide | HCID 2991007 | — |
| Reactant | N-Methoxy-N-methyl-1,3-thiazole-5-carboxamide | HCID 25307138 | — |
| Reactant | (1-Methyl-1H-imidazol-5-yl)(thiazol-5-yl)methanone | HCID 86715592 | — |
| Product | (1-Methyl-1H-imidazol-5-yl)(4-nitrophenyl)methanone | HCID 86715600 | — |
Reaction Steps
The title compound was prepared by substituting N-methoxy-N-methylthiazole-5-carboxamide (Intermediate 11: step a) with N-methoxy-N-methyl-4-nitrobenzamide (Intermediate 20: step a) then following the procedure described for the preparation of (1-methyl-1H-imidazol-5-yl)(thiazol-5-yl)methanone (Intermediate 13).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09290476B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-e4a3596e0f244584b74197e096f27796 |
| Source note | uspto-grants-2016_03 |