Trifluoroacetic acid → HCID 59129572, compound

HRID 1847888Notes

Reaction equation

HRID 1847888 reaction equation
FC(F)(F)C(O)=O.[O:8]1[C:12]2[CH:13]=[CH:14][C:15]([C:17]3([C:20]([NH:22][C:23]4[CH:24]=[C:25]5[C:29](=[CH:30][CH:31]=4)[NH:28][C:27]([C:32]([CH3:43])([CH3:42])[CH2:33][NH:34]C(=O)OC(C)(C)C)=[CH:26]5)=[O:21])[CH2:19][CH2:18]3)=[CH:16][C:11]=2[O:10][CH2:9]1>ClCCl>[NH2:34][CH2:33][C:32]([C:27]1[NH:28][C:29]2[C:25]([CH:26]=1)=[CH:24][C:23]([NH:22][C:20]([C:17]1([C:15]3[CH:14]=[CH:13][C:12]4[O:8][CH2:9][O:10][C:11]=4[CH:16]=3)[CH2:19][CH2:18]1)=[O:21])=[CH:31][CH:30]=2)([CH3:42])[CH3:43]

Participants

4

Reactant 2

HCID 6422Trifluoroacetic acidHCID 24763146HCID 24763146, compound

Product 1

HCID 59129572HCID 59129572, compoundYield 86%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

Trifluoroacetic acid (0.75 mL) was added to a solution of tert-butyl 2-(5-(1-(benzo[d][1,3]dioxol-5-yl)cyclopropanecarboxamido)-1H-indol-2-yl)-2-methylpropylcarbamate (77 mg, 0.16 mmol) in dichloromethane (3 mL) and the mixture was stirred at room temperature for 1.5 h. The mixture was evaporated, dissolved in dichloromethane, washed with saturated sodium bicarbonate solution, dried over magnesium sulfate and evaporated to dryness to give N-(2-(1-amino-2-methylpropan-2-yl)-1H-indol-5-yl)-1-(benzo[d][1,3]dioxol-5-yl)cyclopropanecarboxamide (53 mg, 86%). 1H NMR (400 MHz, CDCl3) δ 9.58 (s, 1H), 7.60 (d, J=1.6 Hz, 1H), 7.18-7.15 (m, 2H), 7.02-6.94 (m, 3H), 6.85 (d, J=7.8 Hz, 1H), 6.14 (d, J=1.2 Hz, 1H), 6.02 (s, 2H), 2.84 (s, 2H), 1.68 (dd, J=3.6, 6.7 Hz, 2H), 1.32 (s, 6H), 1.08 (dd, J=3.7, 6.8 Hz, 2H).

Workup

  1. customThe mixture was evaporated
  2. dissolutiondissolved in dichloromethane
  3. washwashed with saturated sodium bicarbonate solution
  4. dry with materialdried over magnesium sulfate
  5. customevaporated to dryness

Sources & evidence

ORD record
ord-6e7b3065d7b14f8896e3277a0d490fa6
Source dataset
uspto-grants-2015_02
Patent number
US08952049B2

Reaction notes

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