Hydrochloric Acid → (S)-2-amino-1-(3,3-difluoro-azetidin-1-yl)-3-methyl-pentan-1-one hydrochloride

HRID 49765

反応式

HRID 49765 の反応式
[ClH:1].[F:2][C:3]1([F:7])[CH2:6][NH:5][CH2:4]1.C([NH:15][C@H:16]([C:21](O)=[O:22])[C@H:17]([CH2:19][CH3:20])[CH3:18])(OC(C)(C)C)=O.Cl>>[ClH:1].[NH2:15][C@@H:16]([CH:17]([CH3:18])[CH2:19][CH3:20])[C:21]([N:5]1[CH2:6][C:3]([F:7])([F:2])[CH2:4]1)=[O:22]

参加物

4

反応物 3

HCID 313Hydrochloric AcidHCID 2724762tert-Butoxycarbonyl-L-isoleucineHCID 27582473,3-Difluoroazetidine hydrochloride

生成物 1

HCID 69713143(S)-2-amino-1-(3,3-difluoro-azetidin-1-yl)-3-methyl-pentan-1-one hydrochloride

実験手順

(S)-2-amino-1-(3,3-difluoro-azetidin-1-yl)-3-methyl-pentan-1-one hydrochloride was prepared by coupling 3,3-difluoro-azetidine hydrochloride (WO 0047582) with Boc-(L)-isoleucine followed by HCl deprotection as analogously described in Example 1 (mp 195° C. dec.).

出典と根拠

ORDレコード
ord-8454b09149134b8bb6599e0436bd96ab
出典データセット
uspto-grants-2004_03
特許番号
US06710040B1

関連ノート

読み込み中…