Triethylamine → HCID 9901478, compound

HRID 428731Notes

Reaction equation

HRID 428731 reaction equation
O[C:2]1C=C[C:5]([C:8]#[C:9][C:10]2[CH:11]=[C:12]3[C:16](=[CH:17][CH:18]=2)[NH:15][C:14](=[O:19])/[C:13]/3=[CH:20]\[C:21]2[NH:22][CH:23]=[CH:24][CH:25]=2)=[CH:4][CH:3]=1.C(C1C=C2C(=CC=1)NC(=O)/C/2=C\C1NC=CC=1)#C.BrC1[S:46]C=CC=1.C(N(CC)CC)C>[Cu]I.Cl[Pd](Cl)([P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.CN(C=O)C>[NH:22]1[CH:23]=[CH:24][CH:25]=[C:21]1/[CH:20]=[C:13]1\[C:14](=[O:19])[NH:15][C:16]2[C:12]\1=[CH:11][C:10]([C:9]#[C:8][C:5]1[S:46][CH:2]=[CH:3][CH:4]=1)=[CH:18][CH:17]=2

Participants

8

Reactant 4

HCID 8471TriethylamineHCID 138512-BromothiopheneHCID 9813420HCID 9813420, compoundHCID 9923369HCID 9923369, compound

Product 1

HCID 9901478HCID 9901478, compound

Reagents, catalysts & solvents 3

HCID 24350Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)CatalystHCID 178418476HCID 178418476, compoundCatalystHCID 6228DimethylformamideSolvent

Procedure

This compound was also prepared in a manner analogous to the preparation of (Z)-1,3-dihydro-5-(4-hydroxyphenyl)ethynyl-3-[(1H-pyrrol-2-yl)methylene]-2H-indol-2-one in Example 83 above. In this example, (Z)-1,3-dihydro-5-ethynyl-3-[(1H-pyrrol-2-yl)methylene]-2H-indol-2-one (42 mg, 0.18 mmol) (from Example 82) was coupled with 2-bromothiophene (30 mg, 0.18 mmol) (Aldrich) using CuI (8 mg, 0.042 mmol) (Aldrich) and (Ph3P)2PdCl2 (14 mg, 0.020 mmol) (Aldrich) as catalyst in 1 mL DMF and 1 mL triethylamine at 70° C. for 14 hours to give (Z)-1,3-dihydro-3-[(1H-pyrrol-2-yl)-methylene]-5-(2-thiophenyl)ethynyl-2H-indol-2-one as a yellow powder. (Yield 25 mg, 44%).

Sources & evidence

ORD record
ord-66e373c1fdb0474689bec5b652e47ad3
Source dataset
uspto-grants-2001_11
Patent number
US06313310B1

Reaction notes

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