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HRID 1504819作成日:2026年10月25日

Methylamine → Benzyl {2-[(tert-butoxycarbonyl)amino]-3-(methylamino)-3-oxopropyl}carbamate

https://huagongshe.com/reaction/1504819

反応式

関与物質

役割名称HCID仕込み量
反応物MethylamineHCID 6329—
反応物TriethylamineHCID 8471—
反応物Boc-dap(Z)-OHHCID 2755950—
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—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物Benzyl {2-[(tert-butoxycarbonyl)amino]-3-(methylamino)-3-oxopropyl}carbamateHCID 69717545—

反応手順

To a solution of 3-{[(benzyloxy)carbonyl]amino}-N-(tert-butoxycarbonyl)alanine (10.0 g, 30.0 mmol) in DMF (100 mL) was added HATU (14.0 g, 36.0 mmol). After 2 hours, methylamine (4.1 g, 60 mmol) and triethylamine (15.0 g, 149 mol) were added. After 16 hours, the reaction mixture was diluted with water and the aqueous layer was extracted with ethyl acetate (3×100 mL). The combined organic layers were dried over sodium sulfate, filtered, and concentrated under reduced pressure. The residue was purified via reverse phase HPLC (acetonitrile/water with 0.1% TFA, linear gradient) to give benzyl {2-[(tert-butoxycarbonyl)amino]-3-(methylamino)-3-oxopropyl}carbamate. MS ESI calc'd. for C17H26N3O5 [M+H]+ 352. found 352. 1H NMR (300 MHz, CDCl3) δ 7.33-7.31 (m, 5H), 6.59-6.57 (m, 1H), 5.69-5.66 (m, 1H), 5.42-5.39 (m, 1H), 5.14-5.05 (m, 2H), 4.19-4.16 (m, 1H), 3.63-3.41 (m, 2H), 2.78 (d, J=4.8 Hz, 3H), 1.43 (s, 9H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09216173B2
出典データセットuspto-grants-2015_12
ORD IDord-79ac8100cb354310b7a6115ed2c35c88
出典メモuspto-grants-2015_12