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HRID 1620962作成日:2026年10月25日

Boron trifluoride etherate → Leucine, N-carboxy-, N-benzyl ester, L-

https://huagongshe.com/reaction/1620962

反応式

関与物質

役割名称HCID仕込み量
反応物Boron trifluoride etherateHCID 8000—
反応物TriethylamineHCID 8471—
反応物(2S)-2-benzyloxycarbonylamino-4-methyl-pentanoic acid 3-methyloxetan-3-ylmethyl esterHCID 67298758—
溶媒DichloromethaneHCID 6344—
生成物Leucine, N-carboxy-, N-benzyl ester, L-HCID 74840—
生成物[3-Methyl-1-(4-methyl-2,6,7-trioxa-bicyclo[2.2.2]oct-1-yl)-butyl]-carbamic acid benzyl esterHCID 67298262—

反応手順

(2S)-2-Benzyloxycarbonylamino-4-methyl-pentanoic acid 3-methyloxetan-3-ylmethyl ester (Cbz-Leu oxetane ester) (2 g, 5.7 mmol) was dissolved in dry CH2Cl2 (10 mL) under nitrogen. BF3.Et2O (40 μl, 0.3 mmol, 0.054 eq.) was diluted in dry CH2Cl2 (1 mL) and added to the reaction flask. The reaction was allowed to warm up to room temperature and stirred for 12 h. Triethylamine (335 μl, 3.3 mmol, 0.58 eq) was added and the reaction was stirred for an additional 30 min., before being concentrated to thick oil. The crude product was redissolved on EtOAc (15 mL), washed with 3% NH4C1 (10 mL), and saturated NaCl (10 mL), dried (MgSO4), and evaporated to dryness. The reaction yielded a colorless thick oil, which crystallized on standing to give [3-methyl-1-(4-methyl-2,6,7-trioxa-bicyclo[2.2.2]oct-1-yl)-butyl]-carbamic acid benzyl ester, (Cbz-Leu-OBO ester).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08772336B2
出典データセットuspto-grants-2014_07
ORD IDord-689c3bf4d2414a059e57b7515fd530b6
出典メモuspto-grants-2014_07