Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2039775Generated: October 30, 2026

Diisopropylethylamine → HCID 25094826, compound

https://huagongshe.com/reaction/2039775

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 59539022HCID 59539022—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 25094826HCID 25094826—

Reaction Steps

BOP (11 g, 24 mmol) is added to a slurry of pyrazolo[1,5-a]pyridine-2,4-dicarboxylic acid 2-ethyl ester (5.6 g, 24 mmol), adamantan-1-ylmethylamine (4.4 g, 27 mmol), iPr2NEt (21 mL, 120 mmol), and DMF (240 mL) under N2. The reaction vessel is sealed and the mixture is left to stir for 15 h. EtOAc (200 mL) is added. The solution is washed with 50% sat. aq. NH4Cl (2×500 mL). The aqueous phases are extracted with EtOAc (3×200 mL). The combined organics are dried over Na2SO4, filtered, and concentrated. Purification by flash column chromatography (2:1 hexanes:EtOAc to 1:1 hexanes:EtOAc) affords the title compound as a tan solid. 1H NMR (400 MHz, CDCl3) δ: 8.62 (d, 1H), 7.60 (d, 1H), 7.44 (s, 1H), 7.00 (t, 1H), 6.23 (bs, 1H), 4.48 (q, 2H), 3.23 (d, 2H), 1.98-2.07 (m, 3H), 1.57-1.78 (m, 12H), 1.45 (t, 3H). LC-MS m/z (M+H+): 382.2; RT=1.09 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580812B2
Source datasetuspto-grants-2013_11
ORD IDord-dbfc92be4c1a4389b0a9953b8d899807
Source noteuspto-grants-2013_11