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HRID 1033408作成日:2026年10月25日

N-((1,1-dimethylethoxy)carbonyl)-2-methyl-alanine → 2-t-Butoxycarbonylamino-2-methyl-N-[2,3,4,5-tetrahydro-2-oxo-1H-benzazepin-3(R)-yl]propanamide

https://huagongshe.com/reaction/1033408

反応式

関与物質

役割名称HCID仕込み量
反応物N-((1,1-dimethylethoxy)carbonyl)-2-methyl-alanineHCID 2733845—
反応物(R)-3-amino-4,5-dihydro-1H-benzo[b]azepin-2(3H)-oneHCID 10103689—
生成物2-t-Butoxycarbonylamino-2-methyl-N-[2,3,4,5-tetrahydro-2-oxo-1H-benzazepin-3(R)-yl]propanamideHCID 10808566—

反応手順

Prepared from 2-(t-butoxycarbonylamino)-2-methylpropanoic acid and 3(R)-amino-2,3,4,5-tetrahydro-1H-[1]benzazepin-2-one (Example 1, Step B) by the procedure described in Example 1, Step F. 1H NMR (200MHz, CDCl3): 1.42 (s,12H), 1.46 (s,3H), 1.90 (m,1H), 2.5-3.0 (m,3H), 4.48 (m,1H), 5.01 (br s,1H), 6.97 (d,8Hz,1H), 7.1-7.3 (m,3H), 7.9 (br s,1H). FAB=MS: calculated for C19H27N3O4 361; found 362 (M+H,30%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05310737
出典データセットuspto-grants-1994_05
ORD IDord-4b250e9289a34e9eb3fd3f51df9795e1
出典メモuspto-grants-1994_05