HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromide ion → HCID 12340648, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromide ion | HCID 259 | — |
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | HCID 12340627 | HCID 12340627 | — |
| Product | HCID 12340648 | HCID 12340648 | — |
Reaction Steps
By following the procedure of Example 75 but using as a starting material the appropriate starting material of formula 3, for example those described in Examples 2 to 41 or the appropriate starting material of formula 1, for example, those described in Examples 42 to 69, together with the appropriate nucleophilic reagent, for instance, sulfuryl chloride or bromide, respective compounds of formulae 3 and 1 in which R2 is halogen are obtained. More specifically exemplified, the use of 4-methyl-8-nitro-4H-pyrrolo-[2,1-c][1,4]benzoxazine-4-acetic acid methyl ester, described in Example 2 gives 1-chloro-4-methyl-8-nitro-4H-pyrrolo[2,1-c][1,4]-benzoxazine-4-acetic acid methyl ester, m.p. 124° - 125° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04035495 |
| Source dataset | uspto-grants-1977_07 |
| ORD ID | ord-2916d37bed4a4c90a0233e81b9f2fb37 |
| Source note | uspto-grants-1977_07 |