戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 535160作成日:2026年10月25日

Diisopropylethylamine → HCID 178473608、化合物

https://huagongshe.com/reaction/535160

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物4-Carboxy-1,2,3-triazoleHCID 140120—
反応物Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
反応物1-Chloroethyl Cyclohexyl CarbonateHCID 11229529—
反応物(2S,4S)-5-Biphenyl-4-yl-4-t-butoxycarbonylamino-2-hydroxymethyl-pentanoic acidHCID 68181177—
溶媒DimethylformamideHCID 6228—
溶媒DimethylacetamideHCID 31374—
生成物HCID 178473608HCID 17847360895%

反応手順

(2S,4S)-5-Biphenyl-4-yl-4-t-butoxycarbonylamino-2-hydroxymethyl-pentanoic acid (50 mg, 120 μmol, 1.0 eq.), DMA (1 mL), DIPEA (0.13 mL, 0.75 mmol) and 1-chloroethyl cyclohexyl carbonate (52 mg, 250 μmol, 2.0 eq.) were combined. The reaction vessel was capped and microwaved at 80° C. for 2 hours. The mixture was dried under vacuum, dissolved in MeCN (2 mL), and combined with 4 M of HCl in dioxane (500 μL). The resulting mixture was stirred at room temperature for 30 minutes. The precipitate was filtered and discarded, and the filtrate containing the intermediate was concentrated down and submitted to next step. 1,2,3-triazole-4-carboxylic acid (14 mg, 120 μmol, 0.5 eq.) and HATU (48 mg, 120 μmol, 1.0 eq) were dissolved in DMF (1 mL) and the resulting solution was stirred for 5 minutes, followed by the addition of DIPEA (44 μL) and the intermediate from last step. The mixture was stirred for 5 minutes. The reaction was quenched with water and the product dried under vacuum. The product was then purified by preparative HPLC to yield the title compound (4.8 mg, 95% purity). MS m/z [M+H]+ calc'd for C30H36N4O7, 565.26. found 565.4.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08853427B2
出典データセットuspto-grants-2014_10
ORD IDord-cad392af103344708c20cbf63db9180e
出典メモuspto-grants-2014_10