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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2279632Generated: October 30, 2026

Diisopropylethylamine → HCID 59579856, compound

https://huagongshe.com/reaction/2279632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantTricyclo(3.3.1.13,7)dec-1-ylmethylamineHCID 86625—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
ReactantHCID 59579909HCID 59579909—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 59579856HCID 59579856—

Reaction Steps

To a mixture of 5-chloro-1-pyrimidin-2-yl-1H-pyrazole-4-carboxylic acid (50 mg, 0.22 mmol) in 1.0 mL of DMF is added sequentially DIEA (0.08 mL, 0.44 mmol), 1-adamantan-1-ylmethan-amine (36 mg, 0.22 mmol), and BOP (115 mg, 0.26 mmol). The resulting mixture is stirred at RT for 18 h. Water (3 mL) is added, and the mixture is extracted with EtOAc (5 mL). The EtOAc layer is dried (Na2SO4), filtered, and evaporated in vacuo to give a reddish/brown oil. Purification by silica gel column chromatography (gradient from 90% EtOAc/hexane to EtOAc) affords the title compound as a light reddish/brown solid. 1H NMR (400 MHz, CDCl3) δ 8.89 (2H, d, J 4.8), 8.28 (1H, s), 7.41 (1H, t, J 4.8), 6.47 (1H, bs), 3.18 (2H, d, J 6), 2.01 (3H, s), 1.69 (6H, m), 1.58 (6H, s). MS (M+1)=372.19; RT=1.31 min. *IC50.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133204B2
Source datasetuspto-grants-2015_09
ORD IDord-f495da4ebf854eff9c8560c39baa36c2
Source noteuspto-grants-2015_09