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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2046975Generated: November 1, 2026

Acetic Acid → HCID 178428324, compound

https://huagongshe.com/reaction/2046975

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantFormaldehydeHCID 712—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 178428323HCID 178428323—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178428324HCID 178428324—

Reaction Steps

To a solution of N6-(2-isopropoxy-5-methyl-4-(piperidin-4-yl)phenyl)-N4-(2-(isopropylsulfonyl)phenyl)-3-methyl-1H-pyrazolo[3,4-d]pyrimidine-4,6-diamine (39 mg, 0.067 mmol) in 5.0 mL of MeOH and 5.0 mL of THF was added drops of AcOH and HCHO [1N in MeOH and THF (v/v: 1/1), 0.12 mmol, 120 μL] sequentially. The reaction mixture was stirred at room temperature for 30 min, then NaB(CN)H3 (6.6 mg, 0.12 mmol) was added and the reaction mixture was stirred for another 1 h. Saturated aqueous NH4Cl was added to the reaction and the reaction mixture was concentrated in vacuo. The crude was partitioned between EtOAc and brine. The organic extracts were concentrated and purified by RP-HPLC to afford N6-(2-isopropoxy-5-methyl-4-(1-methylpiperidin-4-yl)phenyl)-N4-(2-(isopropylsulfonyl)phenyl)-3-methyl-1H-pyrazolo[3,4-d]pyrimidine-4,6-diamine. MS (ES+): 592.3 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592432B2
Source datasetuspto-grants-2013_11
ORD IDord-990582ddeb134f7d8d2069c76e809672
Source noteuspto-grants-2013_11