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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1630342Generated: October 30, 2026

Acetohydrazide → Benzoic acid, 5-chloro-2-methoxy-4-[[4-(methylamino)-5-(trifluoromethyl)-2-pyrimidinyl]amino]-, 2-acetylhydrazide

https://huagongshe.com/reaction/1630342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetohydrazideHCID 14039—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 84819816HCID 84819816—
SolventDichloromethaneHCID 6344—
ProductBenzoic acid, 5-chloro-2-methoxy-4-[[4-(methylamino)-5-(trifluoromethyl)-2-pyrimidinyl]amino]-, 2-acetylhydrazideHCID 8668821085%

Reaction Steps

A suspension of 5-chloro-2-methoxy-4-(4-(methylamino)-5-(trifluoromethyl)pyrimidin-2-ylamino)benzoic acid (144 mg, 50% pure material, 0.19 mmol), HATU (85 mg, 0.22 mmol), acetic hydrazide (16 mg, 0.22 mmol) and DIPEA (81 uL, 0.46 mmol) in dichloromethane (4 mL) was stirred at room temperature for 18 h. The mixture was diluted with dichloromethane (10 mL) and washed with saturated aqueous NaHCO3 solution (10 mL). A solid persisted in the aqueous layer; this was filtered, washed with water and then suspended in methanol. The solid was collected by filtration and dried in a vacuum oven to afford N′-acetoyl-5-chloro-2-methoxy-4-(4-(methylamino)-5-(trifluoromethyl)pyrimidin-2-ylamino)benzohydrazide as a white solid (68 mg, 85%). This was taken through to the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791130B2
Source datasetuspto-grants-2014_07
ORD IDord-4f2a8677661f40f8864feef8ddb79bb2
Source noteuspto-grants-2014_07