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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1478284Generated: November 2, 2026

Dimethylformamide → (S)-2-amino-1-(4-(3-bromopyrazolo[1,5-a]pyrimidin-5-yl)piperazin-1-yl)-3-methylbutan-1-one

https://huagongshe.com/reaction/1478284

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantTriethylamineHCID 8471—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant3-Bromo-5-(piperazin-1-yl)pyrazolo[1,5-a]pyrimidineHCID 86697434—
SolventDichloromethaneHCID 6344—
Product(S)-2-amino-1-(4-(3-bromopyrazolo[1,5-a]pyrimidin-5-yl)piperazin-1-yl)-3-methylbutan-1-oneHCID 86697450—

Reaction Steps

3-bromo-5-(piperazin-1-yl)pyrazolo[1,5-a]pyrimidine (400 mg, 1.42 mmol) Boc-L-Leucine (392 mg, 1.7 mmol), HATU (490 mg, 2.13 mmol), and triethylamine (788 uL, 5.7 mmol) taken up in DMF and stirred at room temperature overnight. Reaction diluted with DCM washed with water, DCM layer then dried over magnesium sulfate filtered and reduced in Vacuo. This was then taken up in 26 mL DCM and 4 mL TFA added. Stirred 1 hour until complete by LC/MS. Reaction was washed with 1N NaOH, DCM layer removed dried over magnesium sulfate filtered, reduced in vacuo to obtain 349 mg crude product for further reaction as is. LRMS (ESI) m/z 381/383 [(M+H)]+, calc'd for C15H21BrN6O: 381.28.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403832B2
Source datasetuspto-grants-2016_08
ORD IDord-8290046fd63a4c2aae5d8b9deae79375
Source noteuspto-grants-2016_08