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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968101Generated: October 29, 2026

Triethylamine → HCID 22291587, compound

https://huagongshe.com/reaction/968101

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2,5-Dichloroisonicotinic acidHCID 2736087—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 22291565HCID 22291565—
SolventDimethylformamideHCID 6228—
ProductHCID 22291587HCID 2229158773.4%

Reaction Steps

2,5-Dichloroisonicotinic acid (1.65 g, 0.0086 mol), HATU (3.27 g, 0.0086 mol) and finally Et3N (2.32 mL, 0.0166 mol) were added to a solution of the title compound of step 4 of Example 161 (2 g, 0.00574 mol) in 29 mL of DMF. The reaction mixture was stirred at room temperature for 3 h. The completion of the reaction was confirmed by monitoring the disappearance of the title compound of step 4 of Example 161 in LC/MS. The crude reaction mixture was concentrated to about 10 mL of DMF. Upon addition of water to this DMF residue, a white solid was formed. This white solid was triturated in water for 20 min and filtered. The solid was collected, dissolved in THF, and dried with MgSO4. Removal of the solvent afforded a brown solid that was triturated in warm CH3CN (80° C.) to give 2.2 g of the title compound (yield 73%). Mp: 292-293° C. 1H NMR (300 MHz, d6-DMSO): δ 2.90-2.92 (m, 4H), 6.09 (s, 2H), 6.94-7.04 (m, 2H), 7.12 (d, 1H, J=2 Hz), 7.26-7.38 (m, 4H), 7.51 (s, 1H), 7.81 (s, 1H), 8.61 (s, 1H), 10.54 (s, 1H). M+1=523.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06956052B2
Source datasetuspto-grants-2005_10
ORD IDord-ecee5ba37f1b41e49fa72ec1c93d2306
Source noteuspto-grants-2005_10