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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 897725Generated: October 30, 2026

HCID 20817109, compound → HCID 178437379, compound

https://huagongshe.com/reaction/897725

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 20817109HCID 20817109—
ReactantHCID 178481014HCID 178481014—
ReactantHCID 178514824HCID 178514824—
ProductHCID 178437379HCID 178437379—

Reaction Steps

The boronate intermediate (0.15 g, 0.45 mmol) was coupled with cis-3-iodo-1-[4-(4-methylpiperazino)cyclohexyl]-1H-pyrazolo[3,4-d]pyrimidin-4-amine (0.182 g, 0.41 mmol) using the procedure for Suzuki coupling described in the preparation of N2-(4-{4-amino-1-[4-(4-methylpiperazino)cyclohexyl]-1H-pyrazolo[3,4-d]pyrimidin-3-yl}phenyl)-6-chloro-1,3-benzothiazol-2-amine. Purification of the product by preparative HPLC (25 to 100% acetonitrile in 0.1 M aqueous ammonium acetate over 20 min at 21 mL/min using an 8μ Hypersil HS C18, 250×21 mm column, Rt 7.0-8.0 min) afforded cis-N2-(4-{4-amino-1-[4-(4-methylpiperazino)cyclohexyl]-1H-pyrazolo[3,4-d]pyrimidin-3-yl}phenyl)-4-ethyl-1,3-thiazol-2-amine as an off-white powder (0.069 g, 0.133 mmol); RP-HPLC (25 to 100% acetonitrile in 0.1 M aqueous ammonium acetate over 10 min at 1 mL/min using a 5μ Hypersil HS C18, 250×4.6 mm column) Rt 7.05 min; MS (MH)+ 518.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06921763B2
Source datasetuspto-grants-2005_07
ORD IDord-591502b230cf4c799650896860f894da
Source noteuspto-grants-2005_07