HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 4-Amino-6-chloro-5-(2-methoxy-phenoxy)-2,2'-bipyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 4,6-Dichloro-5-(2-methoxyphenoxy)-2,2'-bipyrimidine | HCID 10545706 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-Amino-6-chloro-5-(2-methoxy-phenoxy)-2,2'-bipyrimidine | HCID 18938906 | — |
Reaction Steps
2.09 g of 4,6-dichloro-5-(2-methoxy-phenoxy)-2,2'-bipyrimidine (EP-A- 0 526 708) were suspended in 75 ml of methanol and 150 ml of ammonia were condensed at 75° C. using a feedpipe. The reaction mixture was left to come to room temperature overnight, concentrated in a water-jet vacuum and the residue was partitioned between a small amount of water and methylene chloride (500 ml). The organic phase was dried over sodium sulphate and concentrated on a rotary evaporator. The residue was triturated with ether, the resulting solid was separated and dried in a high vacuum. The 4-amino-6-chloro-5-(2-methoxy-phenoxy )-2,2'-bipyrimidine was thus obtained as a fine, almost white powder. MS: 329 (M).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05837708 |
| Source dataset | uspto-grants-1998_11 |
| ORD ID | ord-6f5b417188e148ba8f69a679e224e9f7 |
| Source note | uspto-grants-1998_11 |