Acetic Anhydride → HCID 86695456, compound

HRID 525576Notes

Reaction equation

HRID 525576 reaction equation
[NH2:1][CH2:2][C:3]1[N:8]=[CH:7][C:6]([C:9]2[CH:14]=[CH:13][C:12]([C@@H:15]([OH:25])[C@H:16]([NH:19][C:20](=[O:24])[CH:21]([Cl:23])[Cl:22])[CH2:17][F:18])=[CH:11][CH:10]=2)=[CH:5][CH:4]=1.C(N(CC)CC)C.[C:33](OC(=O)C)(=[O:35])[CH3:34]>C(Cl)Cl.O>[C:33]([NH:1][CH2:2][C:3]1[N:8]=[CH:7][C:6]([C:9]2[CH:10]=[CH:11][C:12]([C@@H:15]([OH:25])[C@H:16]([NH:19][C:20](=[O:24])[CH:21]([Cl:23])[Cl:22])[CH2:17][F:18])=[CH:13][CH:14]=2)=[CH:5][CH:4]=1)(=[O:35])[CH3:34]

Participants

6

Procedure

To a stirred solution of crude N-{(1S,2R)-2-[4-(6-Aminomethyl-pyridin-3-yl)-phenyl]-1-fluoromethyl-2-hydroxy-ethyl}-2,2-dichloro-acetamide (30 mg, 0.077 mmol) in CH2Cl2 (2 mL) is added triethyl amine (8 mg, 0.078 mmol) and acetic anhydride (20 mg, 0.198) and the reaction mixture was stirred at room temperature for 6 h. Diluted with water and extracted with CH2Cl2dried over sodium sulphate and solvent is evaporated in vacuo to give crude, which is purified by silica gel prep TLC using the mobile phase 10% methanol in CH2Cl2 to afford title compound (5 mg): 1H-NMR (400 MHz, DMSO-d6) 8: (s, 3H), 4.30-4.34 (m, 1H), 4.45 (d, J=5.96 Hz, 2H), 4.48-4.51 (m, 1H), 4.55-4.58 (m, 1H), 5.00 (d, 1H), 5.95 (d, 1H), 6.12 (s, 1H), 6.99 (bs, 1H), 7.34-7.36 (m, 1H), 7.47-7.50 (m, 2H), 7.62-7.67 (m, 2H), 7.96 (dd, J1=8.2 Hz, J2=2.4 Hz, 1H), 8.76 (d, J=2.2 Hz, 1H). LC-Ms (m/z): [M+H]=428.10.

Workup

  1. extractionextracted with CH2Cl2dried over sodium sulphate and solvent
  2. customis evaporated in vacuo
  3. customto give crude, which
  4. customis purified by silica gel prep TLC

Sources & evidence

ORD record
ord-216806d8aa354f37b7053e22e886100d
Source dataset
uspto-grants-2016_05
Patent number
US09340564B2

Reaction notes

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