反応式
Cl.[N:2]1([CH:8]2[CH2:13][CH2:12][N:11]([C:14]([Cl:16])=[O:15])[CH2:10][CH2:9]2)[CH2:7][CH2:6][CH2:5][CH2:4][CH2:3]1.C([O-])([O-])=O.[K+].[K+]>C(Cl)Cl>[N:2]1([CH:8]2[CH2:9][CH2:10][N:11]([C:14]([Cl:16])=[O:15])[CH2:12][CH2:13]2)[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7]1参加物
4
実験手順
[1,4′]bipiperidinyl-1′-carbonyl chloride hydrochloride (9.7 g), methylene chloride (150 ml) and K2CO3 (10.5 g, 2.1 ekv) were charged. The mixture was stirred for about 1 hour. The solution was filtered and the cake washed with 10 ml of methylene chloride. The solution (containing 8.4 g of [1,4′]bipiperidinyl-1′-carbonyl chloride) can be used as such for the preparation of Irinotecan
後処理
- filtrationThe solution was filtered
- washthe cake washed with 10 ml of methylene chloride
- additionThe solution (containing 8.4 g of [1,4′]bipiperidinyl-1′-carbonyl chloride)
- customsuch for the preparation of Irinotecan
出典と根拠
- ORDレコード
- ord-8b865cb372234e82bd5519d0c0b4537c
- 出典データセット
- uspto-grants-2010_02
- 特許番号
- US07662964B2
関連ノート
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