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HRID 400935作成日:2026年10月25日

3,3,4,4-Tetrafluoropyrrolidine Hydrochloride → 5-tert-Butyl-3-(4-methoxy-benzyl)-7-(3,3,4,4-tetrafluoro-pyrrolidin-1-yl)-3H-[1,2,3]triazolo[4,5-d]pyrimidine

https://huagongshe.com/reaction/400935

反応式

関与物質

役割名称HCID仕込み量
反応物3,3,4,4-Tetrafluoropyrrolidine HydrochlorideHCID 22645920—
反応物4-(5-tert-butyl-3-(4-methoxy benzyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidin-7-yl)morpholineHCID 71558051—
反応物5-tert-butyl-7-chloro-3-(4-methoxybenzyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidineHCID 86683299—
生成物5-tert-Butyl-3-(4-methoxy-benzyl)-7-(3,3,4,4-tetrafluoro-pyrrolidin-1-yl)-3H-[1,2,3]triazolo[4,5-d]pyrimidineHCID 86683345—

反応手順

In analogy to the procedure described for the synthesis of 4-(5-tert-butyl-3-(4-methoxybenzyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidin-7-yl)morpholine (example 58, step c), the title compound was prepared from 5-tert-butyl-7-chloro-3-(4-methoxybenzyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidine and 3,3,4,4-tetrafluoropyrrolidine hydrochloride and used without further purification in the consecutive step.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08741906B2
出典データセットuspto-grants-2014_06
ORD IDord-f5070ca88c8e4c6285634bcdd5c4188c
出典メモuspto-grants-2014_06