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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 920731Generated: October 31, 2026

Dimethylformamide → 2-(3-Chloro-4-fluorophenyl)-N5-(2-methyl-1-(trifluoromethoxy)propan-2-yl)-6,7-dihydropyrazolo[1,5-a]pyrazine-3,5(4H)-dicarboxamide

https://huagongshe.com/reaction/920731

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant2-(3-Chloro-4-fluorophenyl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazine-3-carboxamideHCID 118061627—
Reactant3-(Trifluoromethoxy)cyclobutane-1-carboxylic acidHCID 118061739—
SolventTolueneHCID 1140—
Product2-(3-Chloro-4-fluorophenyl)-N5-(2-methyl-1-(trifluoromethoxy)propan-2-yl)-6,7-dihydropyrazolo[1,5-a]pyrazine-3,5(4H)-dicarboxamideHCID 1180614607%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a stirred solution of Intermediate 212C (95 mg, 0.509 mmol) in toluene (5 ml) was added TEA (0.118 mL, 0.848 mmol), DPPA (0.047 mL, 0.204 mmol) and the reaction mixture was stirred at 90° C. for 1 h. The reaction mixture was cooled RT and to it was added a solution of Intermediate 185B (50 mg, 0.170 mmol) in DMF (2 ml) and stirred at RT for 16 h. The reaction was quenched with a 10% aqueous solution of NaHCO3 and extracted with EtOAc (2×20 mL). The combined organic layer dried over Na2SO4, filtered and the filtrate evaporated. The crude compound was purified by preparative HPLC to afford Compound 212 as an off-white solid (6 mg, 7% yield). HPLC retention times 9.95 min. and 9.08 min. (Methods A and B respectively). MS(ES): m/z 478 [M+H]+; 1H NMR (400 MHz, MeOH-d1) δ ppm 7.75-7.77 (m, 1H), 7.58-7.62 (m, 1H), 7.29-7.33 (t, J=8.84 Hz, 1H), 4.85 (s, 2H), 4.23 (s, 2H), 4.18-4.21 (t, J=5.24 Hz, 2H), 3.90-3.92 (t, J=5.24 Hz, 2H), 1.37 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273058B2
Source datasetuspto-grants-2016_03
ORD IDord-9f57b9e43c4e40b5bdcda860fae86d4e
Source noteuspto-grants-2016_03