N-methyl-2-pyrrolidone → 5-Phenylthiophen-3-amine

HRID 1611478Notes

Reaction equation

HRID 1611478 reaction equation
[NH2:1][C:2]1[CH:6]=[C:5]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)[S:4][C:3]=1C(OC)=O.CN1CCNCC1.CN1CCCC1=O>O>[C:7]1([C:5]2[S:4][CH:3]=[C:2]([NH2:1])[CH:6]=2)[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=1

Participants

5

Conditions

Temperature
160 °C

Procedure

A mixture of methyl 3-amino-5-phenylthiophene-2-carboxylate (2.50 g, 10.7 mmol), 3.5 mL of N-methylpiperazine and 12 mL of N-methylpyrrolidinone is heated at 160° C. for 4 hours. The reaction mixture is cooled to room temperature and poured into 100 mL of water. The solids are collected by filtration washing with 50 mL of water. Ethyl acetate and hexane are added and the filtrate is decanted off from the gummy black residue. The filtrate is concentrated to provide 850 mg of 5-phenyl-3-thienylamine as a yellow solid, mp 76-78° C.; 1H NMR (DMSO-d6) δ 4.87 (s, 2H), 5.98 (d, J=1.5 Hz, 1H), 6.95 (d, J=1.5 Hz, 1H), 7.28 (m, 1H), 7.37 (t, J=7 Hz, 2H), 7.53 (d, J=7 Hz, 2H); MS 176.2 (M+H)+.

Workup

  1. temperatureThe reaction mixture is cooled to room temperature
  2. filtrationThe solids are collected by filtration
  3. washwashing with 50 mL of water
  4. additionEthyl acetate and hexane are added
  5. customthe filtrate is decanted off from the gummy black residue
  6. concentrationThe filtrate is concentrated

Sources & evidence

ORD record
ord-9fde6d4e30794b4183a9820d206628ce
Source dataset
uspto-grants-2006_01
Patent number
US06987116B2

Reaction notes

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