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HRID 400856作成日:2026年10月25日

1-(Bromomethyl)-3-chlorobenzene → 5-tert-Butyl-3-(3-chloro-benzyl)-7-(3,3-difluoro-pyrrolidin-1-yl)-3H-[1,2,3]triazolo[4,5-d]pyrimidine

https://huagongshe.com/reaction/400856

反応式

関与物質

役割名称HCID仕込み量
反応物1-(Bromomethyl)-3-chlorobenzeneHCID 69838—
反応物5-tert-Butyl-7-(3,3-difluoro-pyrrolidin-1-yl)-3-ethyl-3H-[1,2,3]triazolo[4,5-d]pyrimidineHCID 71558205—
反応物HCID 178441789HCID 178441789—
生成物5-tert-Butyl-3-(3-chloro-benzyl)-7-(3,3-difluoro-pyrrolidin-1-yl)-3H-[1,2,3]triazolo[4,5-d]pyrimidineHCID 71558206—

反応手順

In analogy to the procedure described for the synthesis of 5-tert-butyl-7-(3,3-difluoro-pyrrolidin-1-yl)-3-ethyl-3H-[1,2,3]triazolo[4,5-d]pyrimidine (example 61), the title compound was prepared from 5-tert-butyl-7-(3,3-difluoropyrrolidin-1-yl)-3H-[1,2,3]triazolo[4,5-d]pyrimidine and 1-(bromomethyl)-3-chlorobenzene and isolated as light-yellow gum (7.0 mg, 42%). MS (m/e): 407.4 (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-d12dfb59d9ca45d8b019077dadf5e573
出典メモuspto-grants-2014_06