HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Methylethylamine → N'-(4-Bromophenyl)-N-ethyl-N-methyl-methanesulfonimidamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Methylethylamine | HCID 12219 | — |
| Reactant | N-(4-Bromophenyl)methanesulfinamide | HCID 14195208 | — |
| Product | N'-(4-Bromophenyl)-N-ethyl-N-methyl-methanesulfonimidamide | HCID 118863958 | — |
Reaction Steps
The title compound is prepared from N-(4-bromophenyl)methanesulfinamide and methylethylamine following a procedure analogous to that described for Intermediate 3 (Step 2). LC (method 1): tR=0.99 min; Mass spectrum (ESI+): m/z=291, 293 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09422312B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-a8edcd2086114f08841cc61df80eee51 |
| Source note | uspto-grants-2016_08 |