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HRID 1602245作成日:2026年10月25日

Acetic Acid → 3-(3-Chloro-4-methoxy-benzylamino)-4-(3-chloro-phenylamino)-1H-pyrazolo[3,4-d]pyrimidine

https://huagongshe.com/reaction/1602245

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物3-Chloro-4-methoxybenzaldehydeHCID 78619—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物HCID 178509242HCID 178509242—
溶媒MethanolHCID 887—
溶媒1,3-Dimethyl-2-imidazolidinoneHCID 6661—
生成物3-(3-Chloro-4-methoxy-benzylamino)-4-(3-chloro-phenylamino)-1H-pyrazolo[3,4-d]pyrimidineHCID 19610550—

反応手順

Analogously to Example 21, 1.00 mmol of 3-amino-4-(3-chloro-phenylamino)-1H-pyrazolo[3,4-d]pyrimidine in 26 ml of methanol, 13 ml of DMEU and 3.0 mmol of acetic acid are first reacted with 3-chloro-4-methoxy-benzaldehyde and then reduced with 7.00 mmol of NaCNBH3 (5-7 days). 3-(3-Chloro-4-methoxy-benzylamino)-4-(3-chloro-phenylamino)-1H-pyrazolo[3,4-d]pyrimidine is obtained; m.p. 205-208° C.; HPLC: TRet (Grad20-100)=12.2.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05981533
出典データセットuspto-grants-1999_11
ORD IDord-9803bff3c783425c808218ddbf3b0f95
出典メモuspto-grants-1999_11