Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1912470Generated: October 31, 2026

Ammonia → HCID 66825610, compound

https://huagongshe.com/reaction/1912470

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantMethanolHCID 887—
ReactantHCID 86690809HCID 86690809—
SolventWaterHCID 962—
SolventSodium CarbonateHCID 10340—
ProductHCID 66825610HCID 6682561082.1%

Reaction Conditions

Temperature60 °C

Reaction Steps

32% aqueous ammonia solution (11.9 mL, 201.1 mmol) was added to a stirred mixture of (R)-4-(3-bromo-phenyl)-4-methyl-4,5-dihydro-pyrazolo[1,5-a]pyrazine-6-thione (1.8 g, 5.59 mmol) in 7 N solution of ammonia in methanol (11.97 mL, 83.79 mmol) in a sealed tube. The mixture was stirred at 60° C. for 90 minutes. After cooling to room temperature the mixture was diluted with water and Na2CO3 (aq. sat. solution) and extracted with DCM. The organic layer was separated, dried (Na2SO4), filtered and the solvents evaporated in vacuo. The crude product was purified by flash column chromatography (silica gel; 7 M solution of ammonia in methanol in DCM 0/100 to 2/98 to 3/97 to 10/90). The desired fractions were collected and concentrated in vacuo to yield (R)-4-(3-bromo-phenyl)-4-methyl-4,7-dihydro-pyrazolo[1,5-a]pyrazin-6-ylamine (1.4 g, 82% yield) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609660B2
Source datasetuspto-grants-2013_12
ORD IDord-a747c58991784e498b51eb7a760493f2
Source noteuspto-grants-2013_12