Hydrochloride methanol → 1260081-87-5
反応式
CO.Cl.[N:4]1[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][C:12]=2[S:14]([NH:17][C:18]2[CH:38]=[CH:37][C:21]([C:22]([N:24]3[CH2:29][CH2:28][N:27](C(OC(C)(C)C)=O)[CH2:26][CH2:25]3)=[O:23])=[CH:20][CH:19]=2)(=[O:16])=[O:15])[CH:7]=[CH:6][CH:5]=1>>[N:24]1([C:22]([C:21]2[CH:20]=[CH:19][C:18]([NH:17][S:14]([C:12]3[CH:11]=[CH:10][CH:9]=[C:8]4[C:13]=3[N:4]=[CH:5][CH:6]=[CH:7]4)(=[O:16])=[O:15])=[CH:38][CH:37]=2)=[O:23])[CH2:29][CH2:28][NH:27][CH2:26][CH2:25]1参加物
3
実験手順
To a solution of MeOH.HCl, Boc protected amine 138 (2 gm, 4.03 mmol) was added and the resulting mixture was stirred for 1 hr. After completion of reaction, solvent was removed under reduced pressure, washed with water followed by addition of NaHCO3 and extracted with DCM. The organic layer was dried over Na2SO4 and evaporated under reduced pressure to afford product 139 (1.5 gm, 94.30% yield).
後処理
- additionwas added
- customAfter completion of reaction, solvent
- customwas removed under reduced pressure
- washwashed with water
- additionfollowed by addition of NaHCO3
- extractionextracted with DCM
- dry with materialThe organic layer was dried over Na2SO4
- customevaporated under reduced pressure
出典と根拠
- ORDレコード
- ord-0363432c785a43418848cd69490da63a
- 出典データセット
- uspto-grants-2014_07
- 特許番号
- US08785450B2
反応ノート
読み込み中…