HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 897725Generated: October 30, 2026
HCID 20817109, compound → HCID 178437379, compound
https://huagongshe.com/reaction/897725
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 20817109 | HCID 20817109 | — |
| Reactant | HCID 178481014 | HCID 178481014 | — |
| Reactant | HCID 178514824 | HCID 178514824 | — |
| Product | HCID 178437379 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06921763B2 |
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| Source dataset | uspto-grants-2005_07 |
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| ORD ID | ord-591502b230cf4c799650896860f894da |
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| Source note | uspto-grants-2005_07 |
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