HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromopropiophenone → 2-Amino-4-phenyl-5-methylthiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromopropiophenone | HCID 16452 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Product | 2-Amino-4-phenyl-5-methylthiazole | HCID 96129 | — |
Reaction Steps
Reaction of a α-substituted-α-bromoacetophenone with thiourea or substituted thiourea, at elevated temperatures may give gave an intermediate G1. Suitably, this reaction may be performed under refluxing conditions in the presence of DMF (dimethylformamide). This intermediate (G1) may be reacted with chlorosulfonic acid to yield the sulfonyl chloride B-1. For example 2-bromopropiophenone may be reacted with thiourea to yield 2-amino-5-methyl-4-phenylthiazole, which can be further transformed to 4-(2-amino-5-methylthiazol-4-yl)phenyl sulfonyl chloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07763641B2 |
| Source dataset | uspto-grants-2010_07 |
| ORD ID | ord-fc63787a9d83469284a279a6c0b45bd9 |
| Source note | uspto-grants-2010_07 |