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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 633693Generated: October 29, 2026

Isopropanol → HCID 178505343, compound

https://huagongshe.com/reaction/633693

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
ReactantMethanesulfonic AcidHCID 6395—
Reactant2-Amino-4-(trifluoromethyl)pyrimidineHCID 595915—
CatalystPalladiumHCID 23938—
SolventWaterHCID 962—
ProductHCID 178505343HCID 17850534396%

Reaction Steps

A mixture of 6 g of 10% Pd/C and 60 g (370 mmol) of 2-amino-4-(trifluoromethyl)pyrimidine dissolved in 80 mL of water, 250 mL of isopropanol and 24 mL (370 mmol) of methanesulfonic acid is hydrogenated at 5 bar, at 40° C., for 5 hours in an autoclave. The resulting mixture is then filtered and rinsed with isopropanol and with water. The filtrate is then concentrated under reduced pressure and the residue obtained is dried under vacuum to give 93.5 g of 4-trifluoromethyl-1,4,5,6-tetrahydropyrimidin-2-ylamine methanesulfonate in the form of a white solid. The white solid is dissolved in 250 mL of methyl isobutyl ketone. 100 mL of 10 N sodium hydroxide are then added. The mixture is stirred at room temperature for 15 minutes. The phases are separated by settling and the aqueous phase is re-extracted with methyl isobutyl ketone. The organic phases are combined and then evaporated under vacuum. 59.50 g of 4-trifluoromethyl-1,4,5,6-tetrahydropyrimidin-2-ylamine are thus obtained, the characteristics of which are as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321790B2
Source datasetuspto-grants-2016_04
ORD IDord-db56d57533004ebdb308f6f2986579af
Source noteuspto-grants-2016_04