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HRID 1641945作成日:2026年10月25日

(3R)-3-(Pyrrolidin-1-YL)pyrrolidine → HCID 66736872、化合物

https://huagongshe.com/reaction/1641945

反応式

関与物質

役割名称HCID仕込み量
反応物(3R)-3-(Pyrrolidin-1-YL)pyrrolidineHCID 7176272—
反応物(1R,2S,3R,5S)-3-[6-(2,2-diphenyl-ethylamino)-2-(2-piperidin-1-yl-ethylamino)-purin-9-yl]-5-(4-hydroxymethyl-pyrazol-1-yl)-cyclopentane-1,2-diol trifluoro-acetateHCID 66735860—
反応物(1R,2S,3R,5S)-3-[2-chloro-6-(2,2-diphenyl-ethylamino)-purin-9-yl]-5-(5-ethyl-tetrazol-2-yl)-cyclopentane-1,2-diolHCID 86622803—
生成物HCID 66736872HCID 66736872—

反応手順

This compound is prepared from (1R,2S,3R,5S)-3-[2-chloro-6-(2,2-diphenyl-ethylamino)-purin-9-yl]-5-(5-ethyl-tetrazol-2-yl)-cyclopentane-1,2-diol (Intermediate BA6) using a procedure analogous to that of (1R,2S,3R,5S)-3-[6-(2,2-diphenyl-ethylamino)-2-(2-piperidin-1-yl-ethylamino)-purin-9-yl]-5-(4-hydroxymethyl-pyrazol-1-yl)-cyclopentane-1,2-diol trifluoroacetate (Example 46) by replacing 1-(2-amino-ethyl)piperidine with (R)-[1,3′]bipyrrolidinyl (intermediate EB). MS (ES+) m/e 650.42 (MH+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08114877B2
出典データセットuspto-grants-2012_02
ORD IDord-df640f2932ca4598abffe71569f0a4e5
出典メモuspto-grants-2012_02