Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 5,6-Dichloro-2-cyclopropylpyrimidine-4-carboxylic acid | HCID 58220806 | — |
| Solvent | Water | HCID 962 | — |
| Product | Aminocyclopyrachlor | HCID 17747875 | — |
Reaction Steps
A mixture of 5,6-dichloro-2-cyclopropyl-4-pyrimidinecarboxylic acid (i.e. the product of Step C1 or C2) (280 g, 1.2 mol), water (1.26 L) and aqueous ammonia (28%, 350 g, 5.76 mol) was heated at 80° C. for 5 h. The solution was concentrated at 50° C. and 70 torr (9.3 kPa) pressure to about half volume to remove most of the excess ammonia. The resulting slurry was stirred at 20° C., acidified to pH 1-2 with aqueous hydrochloric acid, cooled to 5° C. and filtered. The isolated solid was dried in a vacuum oven to afford the title product (270 g), a compound of the present invention.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07863220B2 |
|---|
| Source dataset | uspto-grants-2011_01 |
|---|
| ORD ID | ord-01ba197c4f6a4d3aa3f3bdac2f36daae |
|---|
| Source note | uspto-grants-2011_01 |
|---|