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tert-Butyl carbamate → Methyl 5-((tert-butoxycarbonyl)amino)pyrimidine-2-carboxylate

HRID 310
ノート
印刷プレビュー

反応式

HRID 310 の反応式
CC(C)(C)OC(N)=O.COC(=O)c1ncc(Br)cn1>C1COCCO1.CC(=O)O.CC(=O)O.CC1(C)c2cccc(P(c3ccccc3)c3ccccc3)c2Oc2c(P(c3ccccc3)c3ccccc3)cccc21.O=C([O-])[O-].[Cs+].[Cs+].[Pd]>COC(=O)c1ncc(NC(=O)OC(C)(C)C)cn1
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 77922tert-Butyl carbamateHCID 45790831Methyl 5-bromopyrimidine-2-carboxylate

生成物 1

HCID 67980903Methyl 5-((tert-butoxycarbonyl)amino)pyrimidine-2-carboxylate収率 64.27%

試薬・触媒・溶媒 4

HCID 10796Cesium carbonate試薬HCID 6360441,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)触媒
HCID 4144353Palladium (II) acetate触媒
HCID 312751,4-Dioxane溶媒

反応条件

温度
90 °C

実験手順

The methyl 5-bromopyrimidine-2-carboxylate (4 g, 18.43 mmol), tert-butyl carbamate (3.02 g, 25.80 mmol), diacetoxypalladium (0.207 g, 0.92 mmol), (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) (1.066 g, 1.84 mmol), cesium carbonate (9.01 g, 27.65 mmol) and dioxane (50 mL) were placed and sealed into a microwave tube. The reaction was degased, purged with argon and heated to 90 °C (oil bath) over a period of 7 hours . The mixture was poured in water, extracted with ethyl acetate (x2). The organic phase was washed with brine, dried over magnesium sulfate and concentrated. The crude product was purified by flash chromatography on silica gel 15-40µm eluting with 5 to 50% ethyl acetate in dichloromethane. The solvent was evaporated to dryness to afford methyl 5-(tert- butoxycarbonylamino)pyrimidine-2-carboxylate (3.00 g, 64.3 %) as a beige solid.

出典と根拠

ORDレコード
ord-f833eea6508044b8abf8f02c39f87010
出典データセット
750 AstraZeneca ELN dataset
元リンク
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反応ノート

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