Trifluoroacetic acid → trans-(Octahydro-quinolin-1-yl)-(5-piperidin-4-yl-thiophen-3-yl)-methanone

HRID 1809063Notes

Reaction equation

HRID 1809063 reaction equation
C(OC([N:8]1[CH2:13][CH2:12][CH:11]([C:14]2[S:15][CH:16]=[C:17]([C:19]([N:21]3[C@H:30]4[C@@H:25]([CH2:26][CH2:27][CH2:28][CH2:29]4)[CH2:24][CH2:23][CH2:22]3)=[O:20])[CH:18]=2)[CH2:10][CH2:9]1)=O)(C)(C)C.C(O)(C(F)(F)F)=O>C(Cl)Cl>[N:21]1([C:19]([C:17]2[CH:18]=[C:14]([CH:11]3[CH2:10][CH2:9][NH:8][CH2:13][CH2:12]3)[S:15][CH:16]=2)=[O:20])[C@H:30]2[C@@H:25]([CH2:26][CH2:27][CH2:28][CH2:29]2)[CH2:24][CH2:23][CH2:22]1

Participants

4

Reactant 2

HCID 6422Trifluoroacetic acidHCID 86646699trans-4-[4-(Octahydro-quinoline-1-carbonyl)-thiophen-2-yl]-piperidine-1-carboxylic acid t-butyl ester

Product 1

HCID 86646700trans-(Octahydro-quinolin-1-yl)-(5-piperidin-4-yl-thiophen-3-yl)-methanoneYield 69.5%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

trans-4-[4-(Octahydro-quinoline-1-carbonyl)-thiophen-2-yl]-piperidine-1-carboxylic acid t-butyl ester (0.09 g, 0.32 mmol) was dissolved in DCM (2 mL) and TFA (1 mL) and the reaction stirred at room temperature for 6 hours. The solvent was evaporated and the residue product was purified by flash chromatography on an SCX-2 cartridge, washing with acetonitrile and then eluting with 2 M ammonia in methanol. The fractions containing the desired product were concentrated under vacuum to give the title compound (0.074 g). LCMS m/z 333.20 [M+H]+ RT=6.23 min (Analytical Method 2). 1H NMR (400 MHz, CHCl3-d): δ 7.2 (s, 1H), 6.9 (s, 1H), 3.7 (m, 1H), 3.5 (m, 1H), 3.4 (m, 1H), 3.2 (m, 2H), 2.9 (m, 1H), 2.7 (m, 2H), 2.2 (m, 1H), 2.0-1.9 (m, 4H) 1.8-1.0 (m, 13H).

Workup

  1. customThe solvent was evaporated
  2. customthe residue product was purified by flash chromatography on an SCX-2 cartridge
  3. washwashing with acetonitrile
  4. washeluting with 2 M ammonia in methanol
  5. additionThe fractions containing the desired product
  6. concentrationwere concentrated under vacuum

Sources & evidence

ORD record
ord-9ed9ac2a12c1411bbb4150a5931aad8f
Source dataset
uspto-grants-2013_01
Patent number
US08362008B2

Reaction notes

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