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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 641696Generated: October 30, 2026

Sodium Hydroxide → HCID 178428544, compound

https://huagongshe.com/reaction/641696

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant2-Amino-4-chloro-6-methylpyrimidineHCID 21810—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium AcetateHCID 517045—
ReactantHCID 178511715HCID 178511715—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductHCID 178428544HCID 17842854485%

Reaction Conditions

Temperature99 °C

Reaction Steps

A suspension mixture of 2-amino-4-chloro-6-methylpyrimidine (144 g, 1.0 mol), trans-4-aminocyclohexanol (140 g, 1.2 mol), AcOH (5 mL) in water (0.6 L) was heated at 99° C. in a 3.0 L flask. After 6 h at same temperature, Sodium acetate (82.0 g, 1 mol) was added to the reaction mixture. After 48 h, at the same temperature aq NaOH (50 mL, 10 N) was added. The reaction mixture was heated to 99° C. for 2 additional days. The reaction can be stopped if 2-amino-4-chloro-6-methylpyrimidine is less than 2% by HPLC analysis. If the reaction is slow another portion of aq. NaOH can be added to the reaction mixture as long as the pH is ˜7 to 8. The reaction mixture was then neutralized with Sodium bicarbonate and cooled to 0° C. Filtration gave trans-4-(2-amino-6-methylpyrimidin-4-ylamino)cyclohexanol (˜85%). Wet material is used for next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07696213B2
Source datasetuspto-grants-2010_04
ORD IDord-cd01c75745724333874deb9f21b19d71
Source noteuspto-grants-2010_04