HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 879469Generated: October 31, 2026
1-Isopropylpiperazine → HCID 86700282, compound
https://huagongshe.com/reaction/879469
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Isopropylpiperazine | HCID 78013 | — |
| Reactant | HCID 86700283 | HCID 86700283 | — |
| Catalyst | Hexadecyltrimethylammonium Bromide | HCID 5974 | — |
| Catalyst | Potassium Hydroxide | HCID 14797 | — |
| Catalyst | HCID 178418851 | HCID 178418851 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 86700282 | HCID 86700282 | — |
Reaction Steps
In a 5 mL microwave reaction tube, (S)-methyl 2-(2-(4-bromothiazol-2-yl)-7-(4-chlorophenyl)-5-methylbenzo[d]thiazol-6-yl)-2-tert-butoxyacetate (50 mg, 0.08 mmol), isopropylpiperazine (34 mg, 3 eq.), Bis(tri-t-butylphosphine)palladium(0) (3 mg, 15%), cetyltrimethylammonium bromide (4 mg, 0.5 eq.) were charged with 1 mL toluene, then 1 drop of 50% KOH aqueous solution (excess) was added. The reaction was heated to 105° C. for 1 hour. Reaction mixture was purified by HPLC (0.1% TFA in ACN and water) to give desired product. LCMS-ESI+: calc'd for C31H38ClN4O3S2: 613.2 (M+H+); Found: 613.4 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08987250B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-0c6bb3df8ff3469eabf423ce2a0b9443 |
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| Source note | uspto-grants-2015_03 |
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