HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 384257Erstellt: 25. Oktober 2026
m-Aminoacetanilide → 2-(3-acetamidophenylamino)-4-(1-methyl-1H-indol-4-ylamino)pyrimidine-5-carboxamide
https://huagongshe.com/reaction/384257
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | m-Aminoacetanilide | HCID 7604 | — |
| Edukt | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Edukt | 2-(1H-benzo[d][1,2,3]triazol-1-yloxy)-4-(1-methyl-1H-indol-4-ylamino)pyrimidine-5-carboxamide | HCID 57472013 | — |
| Lösungsmittel | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Produkt | 2-(3-acetamidophenylamino)-4-(1-methyl-1H-indol-4-ylamino)pyrimidine-5-carboxamide | HCID 58098914 | 32,1% |
Reaktionsschritte
To a solution of 2-(1H-benzo[d][1,2,3]triazol-1-yloxy)-4-(1-methyl-1H-indol-4-ylamino)pyrimidine-5-carboxamide (60 mg, 0.15 mmol) in NMP (0.6 mL) was added 3-acetamidoaniline (25 mg, 0.165 mmol) and pTsOH.H2O (28 mg, 0.15 mmol). The mixture was heated at 100° C. for 2 h, cooled to room temperature, purified by preparative HPLC to give 2-(3-acetamidophenylamino)-4-(1-methyl-1H-indol-4-ylamino)pyrimidine-5-carboxamide (20 mg). MS found for C22H21N7O2 as (M+H)+ 416.3. λ=211.3, 250.9.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08367689B2 |
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| Quelldatensatz | uspto-grants-2013_02 |
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| ORD ID | ord-36d1eb7dfce843bb91556a2c1b444a69 |
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| Quellennotiz | uspto-grants-2013_02 |
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