HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1821013Generated: November 3, 2026
Phosphorus oxychloride → HCID 68964147, compound
https://huagongshe.com/reaction/1821013
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 68853800 | HCID 68853800 | — |
| Product | HCID 68964147 | HCID 68964147 | 86.8% |
Reaction Steps
In an oven-dried round bottom flask 145 mg (0.35 mmol) of N′-(3-cyano-4-isopropyloxyphenylcarbonyl)-4-bromo-2-methylbenzhydrazide (from EXAMPLE 87, Step A) was combined with 10 mL of anhydrous xylenes and 5 mL of phosphorus oxychloride and the heterogeneous reaction mixture was heated to reflux for 6 h. The resulting homogeneous mixture was cooled down to rt and combined with 200 mL of ice-water, neutralized to pH>10 and extracted with EtOAc (2×150 mL). The combined organic layers were dried with sodium sulfate and solvents were removed under reduced pressure. The crude compound was purified by flash chromatography using Biotage 40S (eluent: hexanes/EtOAc—4/1) to yield 121 mg of title compound: 1H NMR (500 MHZ, CDCl3) δ 1.50 (d, J=7.0, 6H), 2.78 (s, 3H), 4.80 (sep, J=7.0, 1H), 7.14 (d, J=9.0, 1H), 7.54 (dd, J=9.0, 2.0, 1H), 7.58 (d, J=2.0, 1H), 7.91 (d, J=8.5, 1H), 8.30 (d, J=2.0, 1H), 8.33 (dd, J=8.5, 2.0, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07605171B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-f533bd729c0d4d3894dffa7ac61c3855 |
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| Source note | uspto-grants-2009_10 |
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