HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Bromopyrimidine-2-carboxylic acid → 5-bromo-N,N-dimethylpyrimidine-2-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Bromopyrimidine-2-carboxylic acid | HCID 16462970 | — |
| Reactant | 5-bromo-N,N-dimethylpicolinamide | HCID 22831618 | — |
| Product | 5-bromo-N,N-dimethylpyrimidine-2-carboxamide | HCID 59559990 | — |
Reaction Steps
The title compound was prepared in a similar manner as described for Intermediate 161a, from 5-bromopyrimidine-2-carboxylic acid (1.03 g, 5.074 mmol) to give a yellow oil (308 mg, 26% yield). 1H NMR (400 MHz, CDCl3) δ 8.50 (s, 2 H) 3.17 (s, 3 H) 3.00 (s, 3 H); LCMS for C7H8BrN3O m/z 230.00 and 232.00 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07842713B2 |
| Source dataset | uspto-grants-2010_11 |
| ORD ID | ord-dcc375404c884b378aea8c2afc619e58 |
| Source note | uspto-grants-2010_11 |