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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1012151Generated: October 26, 2026

Dimethylformamide → HCID 178486788, compound

https://huagongshe.com/reaction/1012151

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantOxalyl chlorideHCID 65578—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Benzylmorpholine-2-carboxylic acid hydrochlorideHCID 2776352—
ReactantHCID 178486794HCID 178486794—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178486788HCID 17848678810.8%

Reaction Steps

To a suspension of rac-4-benzyl-2-morpholinecarboxylic acid hydrochloride (77 mg, 0.30 mmol) in THF (2 ml) was added DMF (2.0 μl, 0.025 mmol) followed by oxalyl chloride (36 ul, 0.41 mmol). After stirring at room temperature for 20 min. the mixture was evaporated to dryness and then re-suspended in THF (2 ml). A solution of 3-(5,6-dimethoxy-1H-benzimidazol-2-yl)-1H-pyrazol-4-ylamine (60 mg, 0.2 mmol) and diisopropylethylamine (110 μl, 0.9 mmol) in THF (1 ml) was then added and the reaction stirred for at room temperature for 1 h. After 1 h, MeOH (1 ml) was added, the mixture concentrated and the residue purified through preparative LC/MS to give N-[3-(5,6-dimethoxy-1H-benzimidazol-2-yl)-1H-pyrazol-4-yl]-rac-4-benzyl-2-morpholinecarboxamide (AT8769) as a white solid (10 mg, 9%). (LC/MS (basic method): Rt 2.86 min, [M+H]+ 463).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977477B2
Source datasetuspto-grants-2011_07
ORD IDord-61ef1b4438d5482c8fa343a52267a128
Source noteuspto-grants-2011_07