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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 20546Generated: October 27, 2026

Diisopropylethylamine → HCID 178461813, compound

https://huagongshe.com/reaction/20546

Reaction equation

Participants

RoleNameHCIDCharge
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—
ReactantAzetidine hydrochlorideHCID 12308726—
ReactantHCID 178461815HCID 178461815—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 178461813HCID 178461813—

Reaction Steps

A suspension of 4-{3-[(1S)-2-hydroxy-1-methylethoxy]-5-[(1H-pyrazol-3-ylamino)carbonyl]phenoxy}benzoic acid (130 mg, 0.327 mmol), HATU (156 mg, 0.41 mmol), azetidine hydrochloride (38 mg, 0.41 mmol) and DIPEA (0.143 mL; 0.82 mmol) in DMF (2 mL) was stirred at ambient temperature for 16 hours. Water was added to the reaction mixture and it was extracted into ethyl acetate (3×30 mL). The organic phases were combined, washed with brine solution and dried (MgSO4). The filtrate was concentrated in vacuo and the residue chromatographed, eluting with 0-50% methanol in DCM, to give a clear oil which gave a foam under high vacuum (65 mg, 46%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745475B2
Source datasetuspto-grants-2010_06
ORD IDord-56ffacba82354ea1b1d9132faf8ddbd8
Source noteuspto-grants-2010_06