HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1017716Generated: October 31, 2026
O-Phenylenediamine → HCID 18404080, compound
https://huagongshe.com/reaction/1017716
Participants
| Role | Name | HCID | Charge |
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| Reactant | O-Phenylenediamine | HCID 7243 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 22897229 | HCID 22897229 | — |
| Product | HCID 18404080 | HCID 18404080 | — |
Reaction Steps
A mixture of 9-2 (30 mg, 0.12 mmol, 1 equiv) and 1,2-phenylenediamine (39 mg, 0.36 mmol, 3.0 equiv) in polyphosphoric acid (3 mL) was heated at 200° C. for 3 h. The hot reaction mixture was poured into ice water (20 mL), and the resulting mixture was allowed to stand until all polyphosphoric acid had dissolved. The acidic suspension was neutralized with saturated aqueous sodium bicarbonate solution, then extracted with ethyl acetate (2×50 mL). The organic layer were dried over sodium sulfate and concentrated. The residue was suspended in ethyl ether (50 mL) aided by sonication, and the solids were filtered to afford 3-(benzoimidazol-2-yl)-7-chloro-quinolin-2-one (9-3) as a yellow solid. 1H NMR (400 MHz, (CD3)2SO) δ 12.63 (br s, 1H), 12.53 (br s, 1H), 9.13 (s, 1H), 8.01 (d, 1H, J=8.5 Hz), 7.72 (m, 1H), 7.65 (m, 1H), 7.22 (br s, 1H), 7.35 (dd, 1H, J=8.5, 1.9 Hz), 7.21 (m, 2H); HRMS (electrospray FT/ICR) calculated for C16H11N3O [M+H]+ 296.0585, found 296.0590.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06479512B1 |
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| Source dataset | uspto-grants-2002_11 |
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| ORD ID | ord-822b0a1d14cf4799a7ef33e9ad4d0bcf |
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| Source note | uspto-grants-2002_11 |
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