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tert-Butyl piperazine-1-carboxylate → Tert-butyl 4-(3-chloro-4-cyanophenyl)piperazine-1-carboxylate

HRID 692
ノート
印刷プレビュー

反応式

HRID 692 の反応式
CC(C)(C)OC(=O)N1CCNCC1.N#Cc1ccc(Br)cc1Cl>CC(=O)O.CC(=O)O.Cc1ccccc1.O=C([O-])[O-].[Cs+].[Cs+].[Pd].c1ccc(P(c2ccccc2)c2ccc3ccccc3c2-c2c(P(c3ccccc3)c3ccccc3)ccc3ccccc23)cc1>CC(C)(C)OC(=O)N1CCN(c2ccc(C#N)c(Cl)c2)CC1
参加物反応条件実験手順出典と根拠反応ノート

参加物

7

反応物 2

HCID 143452tert-Butyl piperazine-1-carboxylateHCID 70104204-Bromo-2-chlorobenzonitrile

生成物 1

HCID 56481977Tert-butyl 4-(3-chloro-4-cyanophenyl)piperazine-1-carboxylate収率 47.09%

試薬・触媒・溶媒 4

HCID 10796Cesium carbonate試薬HCID 634876Binap, (A+-)-触媒
HCID 4144353
Palladium (II) acetate
触媒
HCID 1140Toluene溶媒

反応条件

温度
80 °C

実験手順

In a 250 mL round-bottomed dried flask , diacetoxypalladium (0.036 g, 0.16 mmol) was treated with 2,2'-bis(diphenylphosphino)-1,1'-binaphthyl (0.195 g, 0.31 mmol) under nitrogen in toluene (35 mL). The reaction was heated to 80 °C and was stirred for 10 min. To the flask was then added tert-butyl piperazine-1-carboxylate (0.602 g, 3.23 mmol), cesium carbonate (0.527 g, 1.62 mmol), potassium carbonate (0.447 g, 3.23 mmol) and 1,4,7,10,13,16-hexaoxacyclooctadecane (0.085 g, 0.32 mmol). The reaction was then treated with 4-bromo-2-chlorobenzonitrile (0.7 g, 3.23 mmol) and was allowed to stir at 80°C for 5 h. The mixture was then filtered over celite and celite was washed with heptanes. The mixture was condensed under reduced pressure and the crude material was purified on preparative HPLC MS using the short high pH shallow gradient method (Mobile phase: 50-70% B; A: H2O with 10 mM NH4CO3 and 0.375% NH4OH v/v, B: CH3CN, 10 min run) on XBridge Prep C18 OBD, 30x50 mm, 5 mm, Waters reverse phase column, to afford tert-butyl 4-(3-chloro-4-cyanophenyl)piperazine-1-carboxylate (0.490 g, 47.1 %) as a white solid.

出典と根拠

ORDレコード
ord-80eaa5d6e27d4cf78d75715b3843cadc
出典データセット
750 AstraZeneca ELN dataset
元リンク
出典を表示

反応ノート

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