戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2173643作成日:2026年10月25日

5-tert-Butyl-3-(2-chloro-benzyl)-7-morpholin-4-yl-3H-[1,2,3]triazolo[4,5-d]pyrimidine → N-{(R)-1-[5-tert-Butyl-3-(2-chloro-benzyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidin-7-yl]-pyrrolidin-3-yl}-acetamide

https://huagongshe.com/reaction/2173643

反応式

関与物質

役割名称HCID仕込み量
反応物5-tert-Butyl-3-(2-chloro-benzyl)-7-morpholin-4-yl-3H-[1,2,3]triazolo[4,5-d]pyrimidineHCID 1433953—
反応物(3R)-(+)-3-AcetamidopyrrolidineHCID 7016129—
反応物5-tert-butyl-7-chloro-3-(2-chlorobenzyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidineHCID 86683284—
生成物N-{(R)-1-[5-tert-Butyl-3-(2-chloro-benzyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidin-7-yl]-pyrrolidin-3-yl}-acetamideHCID 86683370—

反応手順

In analogy to the procedure described for the synthesis of 5-tert-butyl-3-(2-chlorobenzyl)-7-morpholin-4-yl-3H-[1,2,3]triazolo[4,5-d]pyrimidine (example 1, step c), the title compound was prepared from 5-tert-butyl-7-chloro-3-(2-chlorobenzyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidine and (R)-N-(pyrrolidin-3-yl)acetamide. MS(m/e): 428.3 (MH+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09056866B2
出典データセットuspto-grants-2015_06
ORD IDord-91acbcce7f1249a8a6fd75b1a7b31172
出典メモuspto-grants-2015_06