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Methylamine → N-Methyl-6-nitrobenzo[D]thiazol-2-amine

HRID 298
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HRID 298 반응식
CN.O=[N+]([O-])c1ccc2nc(Br)sc2c1>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]>CNc1nc2ccc([N+](=O)[O-])cc2s1
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참가 물질

7

반응물 2

HCID 6329MethylamineHCID 116230402-Bromo-6-nitrobenzothiazole

생성물 1

HCID 638568N-Methyl-6-nitrobenzo[D]thiazol-2-amine수율 6.19%

시약·촉매·용매 4

HCID 10796Cesium carbonate시약HCID 6360441,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)촉매
HCID 4144353
Palladium (II) acetate
촉매
HCID 312751,4-Dioxane용매

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온도
150 °C

실험 절차

methanamine (0.793 mL, 19.30 mmol), 2-bromo-6-nitrobenzo[d]thiazole (1 g, 3.86 mmol), (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) (0.268 g, 0.46 mmol), cesium carbonate (1.886 g, 5.79 mmol) and diacetoxypalladium (0.043 g, 0.19 mmol) were suspended in 1,4-dioxane (8 mL) and sealed into a microwave tube. The reaction was heated to 150°C for 30 minutes in the microwave reactor and cooled to RT. The crude product was purified by ion exchange chromatography, using an SCX column. The desired product was eluted from the column using 7M NH3/MeOH and pure fractions were evaporated to dryness to afford a crude product. The crude product was purified by flash silica chromatography, elution gradient 0 to 50% DCM in EtOAc. Pure fractions were evaporated to dryness to afford N-methyl-6-nitrobenzo[d]thiazol-2-amine (0.050 g, 6.19 %) as a yellow solid.

출처 및 근거

ORD 기록
ord-ced8329d85d843b9adb25a3a7cf2fe09
출처 데이터셋
750 AstraZeneca ELN dataset
원본 링크
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