HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1246791Generated: October 25, 2026
4-Chloro-2-fluorobenzoyl chloride → HCID 21905770, compound
https://huagongshe.com/reaction/1246791
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Chloro-2-fluorobenzoyl chloride | HCID 2773601 | — |
| Reactant | 6-Chloro-N4-(4-chlorophenyl)pyrimidine-4,5-diamine | HCID 16726311 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 21905770 | HCID 21905770 | — |
Reaction Steps
6-Chloro-N4-(4-chlorophenyl)-pyrimidine-4,5-diamine I-(1A-1)a (6.6 g, 26 mmol) in pyridine (30 ml) was cooled to 0° C. and to it was added 4-chloro-2-fluorobenzoyl chloride (5 g, 26 mmol). The reaction was then allowed to warm to ambient temperature overnight. The heterogeneous reaction was diluted with ethanol (50 ml) and the resulting solid collected by filtration. The solids were slurried in toluene, which was then removed under reduced pressure to remove residual ethanol. The solid was slurried in diethyl ether and then collected by filtration to give I-(7A-91)a (8.3 g, 78%): +ACPI MS (M+1) 409.0; 1H NMR (400 MHz, CD3OD) δ 10.60 (s, 1H), 10.10 (s, 1H), 9.19 (s, 1H), 8.74 (t, J=8.1 Hz, 1H), 8.46–8.40 (m, 3H), 8.28 (dd, J=8.7, 2.1 Hz, 1H), 8.20 (d, J=8.7 Hz, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07129239B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-1800146ac7c349e69101ea3ed85714e4 |
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| Source note | uspto-grants-2006_10 |
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