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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453376Generated: October 25, 2026

Diisopropylamine → 2-methyl-5-nitro-N-(pyrimidin-5-yl)benzamide

https://huagongshe.com/reaction/453376

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantPyrimidin-5-amineHCID 344373—
Reactant2-Methyl-5-nitrobenzoic acidHCID 519683—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
SolventDimethylformamideHCID 6228—
Product2-methyl-5-nitro-N-(pyrimidin-5-yl)benzamideHCID 24823255—

Reaction Steps

In a 2L round bottom flask with mechanical stirring was charged with 2-methyl-5-nitrobenzoic acid (20 g), HATU (38 g) and diisopropylamine (32 mL) in DMF (90 mL). This mixture was stirred for 30 min then pyrimidin-5-amine was added and the reaction was stirred for 18 hr. The LCMS showed complete conversion. DMF was removed under vacuum as much as possible then water was added and a solid precipitated out (use mechanical stirring). The tan solid was filtered and rinsed with water, then taken up in EtOAc, washed with brine, dried over MgSO4, filtered and concentrated down. The crude was taken up in EtOAc and the product 45 precipitated out. This was filtered and the filtrate was concentrated down and taken up in EtOAc/Hex. After standing overnight, more solids were filtered and were combined with the first crop. 2-methyl-5-nitro-N-(pyrimidin-5-yl)benzamide 45 was obtained as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492404B2
Source datasetuspto-grants-2013_07
ORD IDord-8412d5d5f20e47908513066372e957b3
Source noteuspto-grants-2013_07