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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2421056Generated: November 1, 2026

Cyclopropanecarboxylic acid → HCID 24882766, compound

https://huagongshe.com/reaction/2421056

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopropanecarboxylic acidHCID 15655—
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 59025410HCID 59025410—
SolventDimethylformamideHCID 6228—
ProductHCID 24882766HCID 2488276651%

Reaction Steps

To the solution of (3aR,7aR)-1-(1,4′-bipiperidin-4-yl)octahydro-2H-benzimidazol-2-one, 0.25 mmol) in dry DMF (3 mL) was added cyclopropanecarboxylic acid (26 mg, 0.3 mmol) followed by HATU (114 mg, 0.3 mmol) and diisopropylethylamine (0.10 mL, 0.5 mmol) and the mixture was stirred at room temperature for 1 h. The reaction was quenched with water (5 mL) and the solvent was removed in vacuo. Dichloromethane (15 mL) was added and washed with saturated NaHCO3 (10 mL) and brine (10 mL) and dried over Na2SO4. The crude product was purified with high pH prep-LCMS to provide the title compound (48 mg, 51%) as white powder. 1H NMR (400 MHz, METHANOL-D4): δ ppm 0.61-0.81 (m, 4H), 1.16-1.43 (m, 6H), 1.50-1.67 (m, 2H), 1.68-1.98 (m, 8H), 2.13-2.29 (m, 3H), 2.44-2.62 (m, 2H), 2.80-3.10 (m, 5H), 3.48-3.66 (m, 1H), 4.31 (d, J=13.28 Hz, 1H), 4.47 (d, J=13.28 Hz, 1H). MS (M+1): 375.2

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07956069B2
Source datasetuspto-grants-2011_06
ORD IDord-22afd5909b3c449697c2b68014c4751c
Source noteuspto-grants-2011_06