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HRID 400895作成日:2026年10月25日

(3S)-pyrrolidin-3-ol → (S)-1-[5-tert-Butyl-3-(4-methoxy-benzyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidin-7-yl]-pyrrolidin-3-ol

https://huagongshe.com/reaction/400895

反応式

関与物質

役割名称HCID仕込み量
反応物(3S)-pyrrolidin-3-olHCID 2733874—
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(S)-1-[5-tert-Butyl-3-(4-methoxy-benzyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidin-7-yl]-pyrrolidin-3-olHCID 86683311—

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 (S)-pyrrolidin-3-ol and isolated as light-yellow solid. MS (m/e): 383.3 (MH+).

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-9f9273e1e8824924966719d817f59d12
出典メモuspto-grants-2014_06