Tetrabutylammonium Fluoride → 3-Hydroxy-1-[4-(3-methoxyazetidine-1-carbonyl)-1,3-oxazol-2-yl]azetidine

HRID 891813ノート

反応式

HRID 891813 の反応式
[Si]([O:18][CH:19]1[CH2:22][N:21]([C:23]2[O:24][CH:25]=[C:26]([C:28]([N:30]3[CH2:33][CH:32]([O:34][CH3:35])[CH2:31]3)=[O:29])[N:27]=2)[CH2:20]1)(C(C)(C)C)(C1C=CC=CC=1)C1C=CC=CC=1.[F-].C([N+](CCCC)(CCCC)CCCC)CCC>O1CCCC1>[OH:18][CH:19]1[CH2:22][N:21]([C:23]2[O:24][CH:25]=[C:26]([C:28]([N:30]3[CH2:33][CH:32]([O:34][CH3:35])[CH2:31]3)=[O:29])[N:27]=2)[CH2:20]1

参加物

4

反応物 2

HCID 2724141Tetrabutylammonium FluorideHCID 222428403-t-Butyldiphenylsilyloxy-1-[4-(3-methoxyazetidine-1-carbonyl)-1,3-oxazol-2-yl]azetidine

生成物 1

HCID 222430243-Hydroxy-1-[4-(3-methoxyazetidine-1-carbonyl)-1,3-oxazol-2-yl]azetidine収率 60%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

To a solution of 3-t-butyldiphenylsilyloxy-1-[4-(3-methoxyazetidine-1-carbonyl)-1,3-oxazol-2-yl]azetidine (1.49 g, 3.23 mmol) (obtained as described in Reference Example 72(1)) in anhydrous tetrahydrofuran (75 ml) was added a solution of 1.0 M tetra-n-butylammonium fluoride in tetrahydrofuran (3.88 ml, 3.88 mmol) in an ice bath and the mixture was stirred in an ice bath for 1 hour. After checking the completion of the reaction, the mixture was concentrated under reduced pressure. The residue was purified by chromatography on a silica gel column using ethyl acetate:methanol (95:5→9:1) as the eluant to afford 3-hydroxy-1-[4-(3-methoxyazetidine-1-carbonyl)-1,3-oxazol-2-yl]azetidine (486 mg, yield 60%) as a white solid.

後処理

  1. customthe completion of the reaction
  2. concentrationthe mixture was concentrated under reduced pressure
  3. customThe residue was purified by chromatography on a silica gel column

出典と根拠

ORDレコード
ord-7a0c5c4ed5b046d095e24137fa50fb4c
出典データセット
uspto-grants-2006_02
特許番号
US07001897B2

反応ノート

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