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Benzenamine, 3-chloro-, hydrochloride (1:1) → HCID 178507467、化合物
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Benzenamine, 3-chloro-, hydrochloride (1:1) | HCID 67336 | — |
| 反応物 | HCID 178484262 | HCID 178484262 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | HCID 178507467 | HCID 178507467 | — |
反応手順
With the exclusion of moisture, 62 mg (0.38 mmol) of 3-chloro-aniline hydrochloride (see Step 14.4) are added to 92 mg (0.36 mmol) of N'-[3-(4-amino-phenyl)-4-cyano-1H-pyrazol-5-yl]-N,N-dimethylformamidine in 1 ml of methanol and the reaction mixture is boiled under reflux for 28 hours. The light-yellow reaction solution is cooled, concentrated by evaporation and chromatographed (SiO2, methylene chloride/ethanol [10:1]). Crystallization from isopropanol yields 3-(4-amino-phenyl)-4-(3-chloro-phenylamino)-1H-pyrazolo[3,4-d]pyrimidine; TLC: Rf =0.33 (methylene chloride:methanol=10:1); FAB-MS: (M)+ =336; HPLC: TRet (Grad20-100)=9.2, TRet (Grad5-40)=18.8.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05981533 |
| 出典データセット | uspto-grants-1999_11 |
| ORD ID | ord-32e83acf70044d60afe7b9f0b645144e |
| 出典メモ | uspto-grants-1999_11 |