1,2-Dichloroethane → HCID 66606524, compound

HRID 1811030Notes

Reaction equation

HRID 1811030 reaction equation
[Br:1][C:2]1[C:3]([CH3:9])=[C:4]([CH:6]=[CH:7][CH:8]=1)[NH2:5].[F:10][C:11]1[CH:19]=[CH:18][CH:17]=[CH:16][C:12]=1[C:13](O)=[O:14].C1C=NC2N(O)N=NC=2C=1.CCN(C(C)C)C(C)C.C(Cl)CCl>CCOC(C)=O>[Br:1][C:2]1[C:3]([CH3:9])=[C:4]([NH:5][C:13](=[O:14])[C:12]2[CH:16]=[CH:17][CH:18]=[CH:19][C:11]=2[F:10])[CH:6]=[CH:7][CH:8]=1

Participants

7

Procedure

Step 1 A mixture of 3-bromo-2-methylaniline (1.66 mL, 13.4 mmol), 2-fluorobenzoic acid (1.883 g, 13.4 mmol), and HOAT (2.74 g, 20.2 mmol) in EtOAc (60 mL) was treated with DIEA (4.7 mL, 26.9 mmol) and EDC (5.15 g, 26.9 mmol) and the mixture was stirred at rt. After 19 h, the mixture was diluted with EtOAc and washed with water, 1 M hydrochloric acid (twice), NaHCO3 (aq) (twice) and brine, dried and concentrated to provide N-(3-bromo-2-methylphenyl)-2-fluorobenzamide as tan fluffy needles (4.11 g, 99%). 1H NMR (400 MHz, chloroform-d) δ 8.34-8.50 (1 H, m), 8.20 (1 H, td, J=7.9, 1.8 Hz), 7.96 (1 H, d, J=8.1 Hz), 7.50-7.59 (1 H, m), 7.44 (1 H, dd, J=8.0, 0.8 Hz), 7.30-7.37 (1 H, m), 7.21 (1 H, dd, J=12.8, 7.9 Hz), 7.12 (1 H, t, J=8.0 Hz), 2.45 (3 H, s). Mass spectrum m/z 308, 310 (M+H)+.

Workup

  1. washwashed with water, 1 M hydrochloric acid (twice), NaHCO3 (aq) (twice) and brine
  2. customdried
  3. concentrationconcentrated

Sources & evidence

ORD record
ord-39dc5d4a50a941d4b787bd994e73809d
Source dataset
uspto-grants-2013_01
Patent number
US08362065B2

Reaction notes

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