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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356646Generated: October 26, 2026

Ammonia → 4-Amino-6-chloro-5-(2-methoxy-phenoxy)-2,2'-bipyrimidine

https://huagongshe.com/reaction/356646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant4,6-Dichloro-5-(2-methoxyphenoxy)-2,2'-bipyrimidineHCID 10545706—
SolventMethanolHCID 887—
Product4-Amino-6-chloro-5-(2-methoxy-phenoxy)-2,2'-bipyrimidineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05837708
Source datasetuspto-grants-1998_11
ORD IDord-6f5b417188e148ba8f69a679e224e9f7
Source noteuspto-grants-1998_11