2-(2-Methoxyethoxy)-1H-isoindole-1,3(2H)-dione → tert-butyl N-(2-(aminooxy)ethyl)carbamate
反応式
O=C1C2C(=CC=CC=2)C(=O)[N:3]1[O:12][CH2:13][CH2:14][NH:15][C:16](=[O:22])[O:17][C:18]([CH3:21])([CH3:20])[CH3:19].COCCON1C(=O)C2C(=CC=CC=2)C1=O>>[NH2:3][O:12][CH2:13][CH2:14][NH:15][C:16](=[O:22])[O:17][C:18]([CH3:20])([CH3:19])[CH3:21]参加物
3
実験手順
2E was deprotected as previously described in 2A, Step 2 to give tert-butyl 2-(aminooxy)ethylcarbamate (2F, 1.26 g, 58% yield). 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 1.45 (s, 9H) 3.37 (q, J=5.31 Hz, 2H) 3.62-3.85 (m, 2H) 4.90 (br. s., 1H) 5.47 (br. s., 2H).
出典と根拠
- ORDレコード
- ord-2b1e0ddd95614fd19e7ba49713a87d9d
- 出典データセット
- uspto-grants-2011_12
- 特許番号
- US08071766B2
反応ノート
読み込み中…