HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415007Generated: October 28, 2026
HCID 66623351, compound → HCID 178426750, compound
https://huagongshe.com/reaction/415007
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 66623351 | HCID 66623351 | — |
| Reactant | HCID 178512385 | HCID 178512385 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 178426750 | HCID 178426750 | 51.2% |
Reaction Steps
A mixture of 2-phenyl-N-cyano-isourea (50 mg, 0.31 mmol) and [6-(3-amino-prop-1-ynyl)-quinazolin-4-yl]-[3-methyl-4-(6-methyl-pyridin-3-yloxy)-phenyl]-amine (30 mg, 0.076 mmol) in isopropanol (3 mL) was heated at 85° C. in a sealed tube. The reaction was cooled to room temperature after 5 hours. Solvent was removed via rotovap. The residue was then purified by FCC to give the final product (18 mg, 51%) as a light yellow solid. MS ESI (+) m/z 463 (M+1) detected; 1H NMR (400 MHz, deuterated DMSO) □ 9.9 (s, 1H), 8.7 (s, 1H), 8.6 (s, 1H), 8.2 (s, 1H), 7.8 (m, 2H), 7.75 (m, 2H), 7.2 (m, 3H), 7.0 (m, 3H), 4.22 (m, 2H), 2.42 (s, 3H), 2.2 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08088766B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-f95e207759854d1dabcb44207cedcb6b |
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| Source note | uspto-grants-2012_01 |
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