Hydroxylamine → 2-Methyl-1-(propylamino)propan-2-ol
反応式
C(OC(N[C:9]1[CH2:10][C:11](C(O)=O)=[CH:12][C:13]2[CH:19]=CC(C3C=CC(C(N4CCCC4)=O)=CC=3)=C[C:14]=2[N:15]=1)=O)(C)(C)C.N[OH:37]>>[CH3:12][C:13]([OH:37])([CH3:19])[CH2:14][NH:15][CH2:9][CH2:10][CH3:11]参加物
3
実験手順
The following examples 115 and 117 were prepared by the procedures as described in Example 101 (Steps H and I) using (1E,4E)-2-(tert-butoxycarbonylamino)-8-(4-(pyrrolidine-1-carbonyl)phenyl)-3H-benzo[b]azepine-4-carboxylic acid and the appropriate amines (2-methyl-1-(propylamino)propan-2-ol was prepared by the procedure reported in J. Am. Chem. Soc. 1939, 61, 3562) or the hydroxylamine.
後処理
- customThe following examples 115 and 117 were prepared by the procedures
出典と根拠
- ORDレコード
- ord-7f643849ad35424a83ec3931029fae9e
- 出典データセット
- uspto-grants-2016_01
- 特許番号
- US09242964B2
反応ノート
読み込み中…