Trifluoroacetic acid → HCID 59735859, compound

HRID 552602Notes

Reaction equation

HRID 552602 reaction equation
[C:1]([C:3]1[CH:47]=[CH:46][CH:45]=[CH:44][C:4]=1[CH2:5][O:6][C:7]1[CH:8]=[C:9]([CH:31]=[C:32]([O:34][CH2:35][C:36]2[CH:41]=[CH:40][CH:39]=[CH:38][C:37]=2[C:42]#[N:43])[CH:33]=1)[C:10]([NH:12][C:13]1[N:18]=[CH:17][C:16]([N:19]([CH2:27][CH2:28][O:29][CH3:30])C(=O)OC(C)(C)C)=[CH:15][CH:14]=1)=[O:11])#[N:2].FC(F)(F)C(O)=O>ClCCl>[C:42]([C:37]1[CH:38]=[CH:39][CH:40]=[CH:41][C:36]=1[CH2:35][O:34][C:32]1[CH:31]=[C:9]([CH:8]=[C:7]([O:6][CH2:5][C:4]2[CH:44]=[CH:45][CH:46]=[CH:47][C:3]=2[C:1]#[N:2])[CH:33]=1)[C:10]([NH:12][C:13]1[CH:14]=[CH:15][C:16]([NH:19][CH2:27][CH2:28][O:29][CH3:30])=[CH:17][N:18]=1)=[O:11])#[N:43]

Participants

4

Procedure

To a stirred solution of tert-butyl 6-({3,5-di(2-cyanobenzyloxy)benzoyl}amino)pyridin-3-yl(2-methoxyethyl)carbamate (237 mg) in dichloromethane (10 ml) was added trifluoroacetic acid (3 ml). The solution was stirred at ambient temperature for three hours. Volatile material was removed by evaporation. The residue was diluted in DCM (100 ml), washed with 2M sodium Hydroxide (50 ml), brine (50 ml), dried over MgSO4. Volatile material was removed by evaporation to give the title compound (190 mg) as a foam, 1H NMR δ (d6-DMSO): 3.22 (t, 2H), 3.28 (2, 3H), 3.50 (t, 2H), 5.31 (s, 4H), 6.92 (s, 1H), 7.12 (dd, 1H), 7.34 (s, 2H), 7.57 (m, 2H), 7.75 (m, 5H), 7.82 (d, 1H), 7.91 (d, 2H), 10.49 (br s, 1H). MS ES+ 534.41 (M+H)+.

Workup

  1. customVolatile material was removed by evaporation
  2. additionThe residue was diluted in DCM (100 ml)
  3. washwashed with 2M sodium Hydroxide (50 ml), brine (50 ml)
  4. dry with materialdried over MgSO4
  5. customVolatile material was removed by evaporation

Sources & evidence

ORD record
ord-61c807b2aef84dabb6ce368e5f87b275
Source dataset
uspto-grants-2011_05
Patent number
US07951830B2

Reaction notes

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