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HCID 59291169, 화합물 → HCID 68592975, 화합물

HRID 251
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HRID 251 반응식
COc1cc2c(cc1N)N(C(C)=O)CC2.Cc1cnc(Cl)nc1-c1cnn2ccccc12>C1COCCO1.CC(=O)O.CC(=O)O.O=C([O-])[O-].[Cs+].[Cs+].[Pd].c1ccc(P(c2ccccc2)c2ccc3ccccc3c2-c2c(P(c3ccccc3)c3ccccc3)ccc3ccccc23)cc1>COc1cc2c(cc1Nc1ncc(C)c(-c3cnn4ccccc34)n1)N(C(C)=O)CC2
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참가 물질

7

반응물 2

HCID 59291169HCID 59291169, 화합물HCID 594418241-(6-Amino-5-methoxyindolin-1-yl)ethanone

생성물 1

HCID 68592975HCID 68592975, 화합물수율 46.76%

시약·촉매·용매 4

HCID 10796Cesium carbonate시약HCID 634876Binap, (A+-)-촉매
HCID 4144353
Palladium (II) acetate
촉매
HCID 312751,4-Dioxane용매

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온도
90 °C

실험 절차

A mixture of 3-(2-chloro-5-methylpyrimidin-4-yl)pyrazolo[1,5-a]pyridine (400 mg, 1.55 mmol), 1-(6-amino-5-methoxyindolin-1-yl)ethanone (341 mg, 1.55 mmol) and diacetoxypalladium (34.9 mg, 0.16 mmol) 2,2'-bis(diphenylphosphino)-1,1'-binaphthyl (97 mg, 0.16 mmol) cesium carbonate (759 mg, 2.33 mmol) were degassed with nitrogen then dioxane (7 mL) was added to mixture and the solution was degassed under vacuum and placed under nitrogen. The resulting suspension was stirred at 90 °C for 5hours. Control uplc/ms OK Control t.l.c : 100%EtOAc and 5%MeOH/CH2Cl2 After cooling, the mixture was filtered and the filtrate evaporated to dryness after addition of silica gel The crude product was purified by flash chromatography on silica gel 45g Merck column solid injectioneluting with 0 to 10%MeOH/EtOAc. The solvent was evaporated to dryness to afford 1-(5-methoxy-6-(5-methyl-4-(pyrazolo[1,5-a]pyridin-3-yl)pyrimidin-2-ylamino)indolin-1-yl)ethanone (301 mg, 46.8 %) as a orange solid.

출처 및 근거

ORD 기록
ord-019ad9f92b5c40ecbf5416e8a6461063
출처 데이터셋
750 AstraZeneca ELN dataset
원본 링크
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