HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704614Generated: October 31, 2026
Hydrochloric Acid → HCID 15615501, compound
https://huagongshe.com/reaction/704614
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Formanilide | HCID 7671 | — |
| Reactant | 4-Chloro-2-(methanesulfonyl)-6-methoxypyrimidine | HCID 13729225 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 15615501 | HCID 15615501 | 87% |
Reaction Steps
1.8 g of formanilide was dissolved in 50 ml of tetrahydrofuran, and 0.4 g of sodium hydride from which the oily matter had been removed beforehand with n-hexane was slowly added to the resulting solution at 10° to 20° C. while cooling with ice water. To the suspension thus obtained was added 3 3 g of 4-chloro-2-methanesulfonyl-6-methoxypyrimidine, and the mixture was stirred for 1 hour at room temperature. Then, 15 ml of 4N hydrochloric acid was added, and reaction was effected for 1 hour under reflux. The reaction liquid was poured in water, extracted with ether, and the ether layer was washed with water, dried over magnesium sulfate, and then the ether was stripped by concentration The residual crystals were recrystallized from n-hexane, and 4.0 g of 2-anilino-4-chloro-6-methoxypyrimidine was obtained (yield 87%). Melting point: 101°-103° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04988704 |
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| Source dataset | uspto-grants-1991_01 |
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| ORD ID | ord-f8c83e859494465d99a524c2effe22a5 |
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| Source note | uspto-grants-1991_01 |
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