HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 432241Generated: October 26, 2026
m-Tolyl isocyanate → HCID 178425600, compound
https://huagongshe.com/reaction/432241
Participants
| Role | Name | HCID | Charge |
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| Reactant | m-Tolyl isocyanate | HCID 69303 | — |
| Reactant | HCID 178480983 | HCID 178480983 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 178425600 | HCID 178425600 | 301.3% |
Reaction Steps
cis-3-(4-Aminophenyl)-1-[4-(4-methylpiperazino)cyclohexyl]-1H-pyrazolo[3,4-d]pyrimidin-4-amine (50 mg, 0.123 mmol) was dissolved in pyridine (3.5 mL) then cooled to 0° C. m-Tolylisocyanate (18 mg, 0.135 mmol) was added and the reaction was allowed to warm to room temperature over 16 hours. The reaction mixture was concentrated under reduced pressure to yield a pale yellow oil (200 mg). Purification was achieved by RP-HPLC (Waters PrepLC 4000, flow rate: 10 mL/min. λ=254 nm Gradient: 10% to 30% acetonitrile/0.1M aqueous ammonium acetate gradient over 40 minutes; Deltapak C18, 300A, 15 μm, 40×100 mm column). The desired product was collected as a white solid (52 mg). HPLC-RT: 12.58 min. (flow rate: 1 mL/min λ=254 nm Gradient: 5% to 85% acetonitrile/0.1M aqueous ammonium acetate gradient over 20 min.; Deltapak C18, 300A, 5 μm, 150×3.9 mm column); m/z (MH+)=540.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06660744B1 |
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| Source dataset | uspto-grants-2003_12 |
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| ORD ID | ord-86c500f90f40444db63cac1fcbe14c2f |
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| Source note | uspto-grants-2003_12 |
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