HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → HCID 61045603, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | 6-chloro-N-cyclopentylpyridine-3-sulfonamide | HCID 16227304 | — |
| Reactant | 6-chloro-N-phenyl-N-(prop-2-en-1-yl)pyridine-3-sulfonamide | HCID 24419482 | — |
| Product | HCID 61045603 | HCID 61045603 | — |
Reaction Steps
According to Process 10.2, starting with 1 g of 6-chloro-N-cyclopentylpyridine-3-sulfonamide and 0.42 mL of allyl bromide, 1.2 g of 6-chloro-N-phenyl-N-(prop-2-en-1-yl)pyridine-3-sulfonamide are obtained in the form of an orange-coloured oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09359329B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-23594132deb14b4e9e60e4e294d88a26 |
| Source note | uspto-grants-2016_06 |