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HRID 2384949作成日:2026年10月25日

Diisopropylethylamine → HCID 178427511、化合物

https://huagongshe.com/reaction/2384949

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物N-(9-Fluorenylmethoxycarbonyl)-O-tert-butylthreonineHCID 6364643—
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HCID 178427512HCID 178427512—
溶媒DichloromethaneHCID 6344—
溶媒Ethyl AcetateHCID 8857—
生成物HCID 178427511HCID 178427511—

反応手順

H-Lys(Boc)-Pro-Pro-Arg(Pmc)-t-Bu (3.55 g, 3.86 m mmol) was added to a solution of the activated acid prepared from Fmoc-Thr(t-Bu)-OH (1.6 g, 4 mmol) and HATU (1.9 g, 5 mmol) and DIEA (1.29 g, 10 mmol) in dry CH2Cl2 (25 mL) and stirred for 20 h at RT. The reaction mixture was then diluted with ethyl acetate (200 mL) and washed with saturated sodium carbonate (2×200 mL), water (2×200 mL) and dried (sodium sulfate). The solution was filtered and the solvents were removed under reduced pressure to leave behind a paste. The paste was chromatographed over flash silica gel (400 g). Elution with 2% methanol in chloroform furnished the product as a colorless foam. Yield: 3.5 g (70%). m.p. 135-138° C. MS m/z 1298.2 [M+H].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08263739B2
出典データセットuspto-grants-2012_09
ORD IDord-dce879e612714b1596bacea6208ddcf5
出典メモuspto-grants-2012_09