Triethylamine → HCID 67998036, compound

HRID 2040394Notes

Reaction equation

HRID 2040394 reaction equation
[CH3:1][C:2]1([CH3:13])[C:10]2[C:5](=[C:6]([NH2:11])[CH:7]=[CH:8][CH:9]=2)[C@H:4]([CH3:12])[CH2:3]1.C(N(CC)CC)C.[CH3:21][N:22]1[CH:26]=[C:25]([C:27](Cl)=[O:28])[C:24]([C:30]([F:33])([F:32])[F:31])=[N:23]1>CN(C)C1C=CN=CC=1.C1COCC1>[CH3:1][C:2]1([CH3:13])[C:10]2[C:5](=[C:6]([NH:11][C:27]([C:25]3[C:24]([C:30]([F:33])([F:32])[F:31])=[N:23][N:22]([CH3:21])[CH:26]=3)=[O:28])[CH:7]=[CH:8][CH:9]=2)[C@H:4]([CH3:12])[CH2:3]1

Participants

6

Reactant 3

HCID 8471TriethylamineHCID 27945811-methyl-3-(trifluoromethyl)-1H-pyrazole-4-carbonyl chlorideHCID 14535936(3R)-1,1,3-trimethyl-2,3-dihydro-1H-inden-4-amine

Product 1

HCID 67998036HCID 67998036, compoundYield 60.5%

Reagents, catalysts & solvents 2

HCID 142844-(Dimethylamino)pyridineCatalystHCID 8028TetrahydrofuranSolvent2×

Procedure

Into a solution composed of 0.15 g of (R)-1,1,3-trimethyl-4-aminoindane (optical purity: 99% ee), 0.13 g of triethylamine, 5 mg of 4-dimethylaminopyridine and 1 mL of THF, a solution of 0.18 g of 1-methyl-3-trifluoromethylpyrazole-4-carbonyl chloride in THF was dropped under ice cool. The mixture was stirred at room temperature for 15 minutes, then, to the reaction mixture was added ice water, and the mixture was extracted with ethyl acetate. The organic layer was washed with a saturated sodium hydrogen carbonate aqueous solution and saturated saline sequentially, then, dried over magnesium sulfate and concentrated under reduced pressure. The resultant residue was subjected to silica gel column chromatography to obtain 0.18 g of (R)-(−)-N-(1,1,3-trimethylindan-4-yl)-1-methyl-3-trifluoromethylpyrazole-4-carboxamide (hereinafter, referred to as present carboxamide compound (1)) (optical purity: 99% ee).

Workup

  1. temperaturecool
  2. extractionthe mixture was extracted with ethyl acetate
  3. washThe organic layer was washed with a saturated sodium hydrogen carbonate aqueous solution and saturated saline sequentially
  4. dry with materialdried over magnesium sulfate
  5. concentrationconcentrated under reduced pressure

Sources & evidence

ORD record
ord-e87fd21036164eb7b897511f9300e7bb
Source dataset
uspto-grants-2013_11
Patent number
US08580836B2

Reaction notes

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