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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097981Generated: November 2, 2026

Ammonium Chloride → HCID 57504290, compound

https://huagongshe.com/reaction/1097981

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantDiisopropylethylamineHCID 81531—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant4-{[1-(2-chlorophenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-yl]oxy}-5-[(5-methylpyridin-2-yl)amino]-5-oxopentanoic acidHCID 57504289—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57504290HCID 5750429058.5%

Reaction Steps

A solution of 4-{[1-(2-chlorophenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-yl]oxy}-5-[(5-methylpyridin-2-yl)amino]-5-oxopentanoic acid (5.0 mg, 0.011 mmol), ammonium chloride (3.0 mg, 0.054 mmol), DIPEA (7.0 mg, 0.054 mmol) and TBTU (7.0 mg, 0.021 mmol) in THF (1 mL) was stirred at ambient temperature for 3 hrs. Water (1 mL) was added and the reaction mixture was purified by preparative HPLC: Mobile phase A: 100% ACN, Mobile phase B: 5% ACN+95% 0.1M NH4OAc in water; Gradient: 0% A to 50% A over 45 min; Flow: 25 ml/min; UV: 235 nm, to give the title compound (3.0 mg). 1H NMR (500 MHz, CDCl3) δ 9.18 (br s, 1H), 8.59 (s, 1H), 8.42 (s, 1H), 8.16 (d, 1H), 8.09 (s, 1H), 7.64 (m, 1H), 7.53 (m, 4H), 5.94 (s, 1H), 5.75 (br s, 1H), 5.57 (br s, 1H), 2.58 (m, 4H), 2.32 (s, 3H), HRMS: calcd for (M+H+) C22H2135ClN7O3: 466.1394. Found: 467.1426.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143263B2
Source datasetuspto-grants-2012_03
ORD IDord-f4ffcafafa6f47ceacdbd9957f3882c8
Source noteuspto-grants-2012_03