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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2081796Generated: November 1, 2026

2,4-Diamino-6-chloropyrimidine → 6-Chloro-5-[(e)-(4-chlorophenyl)diazenyl]pyrimidine-2,4-diamine

https://huagongshe.com/reaction/2081796

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Diamino-6-chloropyrimidineHCID 67432—
ReactantSodium AcetateHCID 517045—
ReactantBenzenediazonium, 4-chloro-, chlorideHCID 11819533—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product6-Chloro-5-[(e)-(4-chlorophenyl)diazenyl]pyrimidine-2,4-diamineHCID 26776441.4%

Reaction Steps

To a suspens-ion of 4-chloro-2,6-diaminopyrimidine (21.68 g, 0.150 mol) in water (750 ml) and acetic acid (750 ml) was added sodium acetate (300 g). Solution occurred after stirring for 20 minutes, and then the solution of 4-chlorobenzenediazonium chloride (0.166 mol) was added with cooling over 30 minutes at a rate that kept the reaction at 18°. The reacton was stirred overnight at room temperature, and the orange crystals were filtered, washed with water (4×400 ml), and dried in vacuo to give 17.6 g of 6-chloro-5-[(4-chlorophenyl)azo]-2,4-pyrimidinediamine. The mother liquors were cooled to 5° for 20 hours, and the crystals were collected and dried in vacuo to give 6.94 g of additional 6-chloro-5-[(4-chlorophenyl)azo]-2,4-pyrimidineadiamine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05185459
Source datasetuspto-grants-1993_02
ORD IDord-43ccfb56e525434f88fadc70d3f50a23
Source noteuspto-grants-1993_02