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ChemicalBook CAS DataBase List 7H-pyrrolo[2,3-c]pyridazin-4-ol
1269822-97-0

7H-pyrrolo[2,3-c]pyridazin-4-ol synthesis

6synthesis methods
4-hydroxy-7H-pyrrolo[2,3-c]pyridazine-6-carboxylic acid

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7H-pyrrolo[2,3-c]pyridazin-4-ol

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Yield:1269822-97-0 77%

Reaction Conditions:

with sulfolane at 270; for 0.25 h;

Steps:

6.2 Synthesis of 7H-pyrrolo[2,3-c]pyridazin-4-ol (C21).

Tetrahydrothiophene 1,1-dioxide (sulfolane, 50 mL) was heated to 270 °C. Compound C20 (13.0 g, 72.6 mmol) was added portion-wise to the hot solvent; thereaction mixture was maintained at 270 °C for 15 minutes, then immediately cooled to room temperature. Purification via silica gel chromatography (Gradient: 1% to 17% methanol in dichloromethane) afforded the product as a yellow solid. Yield: 7.5 g, 56 mmol, 77%. 1H NMR (400 MHz, DMSO-d6) 12.34 (brs, 1H), 8.10 (brs, 1H), 7.51 (brs, I H), 6.63 (d, J=3.3 Hz, I H).

References:

WO2015/92592,2015,A1 Location in patent:Page/Page column 54; 55

1269822-95-8 Synthesis
methyl 4-hydroxy-7H-pyrrolo[2,3-c]pyridazine-6-carboxylate

1269822-95-8
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7H-pyrrolo[2,3-c]pyridazin-4-ol

1269822-97-0
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1269824-46-5 Synthesis
1269824-46-5

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7H-pyrrolo[2,3-c]pyridazin-4-ol

1269822-97-0
18 suppliers
inquiry