HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354168Generated: November 3, 2026
Phosphorus oxychloride → HCID 11751183, compound
https://huagongshe.com/reaction/2354168
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | (1-Methylcyclopropyl)amine hydrochloride | HCID 12953687 | — |
| Reactant | HCID 66918923 | HCID 66918923 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 11751183 | HCID 11751183 | 39.5% |
Reaction Steps
Phosphorus oxychloride (0.11 ml) was added to a mixture of 4-methyl-3-[6-(4-isopropylpiperazin-1-yl)-4-oxoquinazolin-3(4H)-yl]benzoic acid (0.30 g), 1-methylcyclopropylamine hydrochloride (0.13 g) and pyridine (5 ml) and the resultant was heated to 120° C. for 5 minutes in a microwave (Personal Chemistry Emrys Optimizer with 300 W magnetron). The mixture was evaporated. The residue was partitioned between ethyl acetate and saturated NaHCO3 solution. The organic phase was dried (magnesium sulphate) and evaporated and the residue purified by column chromatography on a silica column using initially methylene chloride and then a 9:1 mixture of methylene chloride and methanol as eluent. There was thus obtained the title compound (0.13 g); NMR Spectrum: (CDCl3) 0.76 (m, 4H), 1.09 (d, 6H), 2.20 (s, 3H), 2.20 (s, 3H), 2.72 (in, 5H), 3.35 (m, 4H), 6.61 (s, 1H), 7.43 (m, 2H), 7.66 (m, 3H), 7.78 (m, 2H); Mass Spectrum: M+H+ 460.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07750154B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-fceeaf0858324decb03a93a424795ba0 |
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| Source note | uspto-grants-2010_07 |
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