Pyridine → HCID 86622010, compound

HRID 1944779Notes

Reaction equation

HRID 1944779 reaction equation
Cl.[NH2:2][OH:3].[CH3:4][C@H:5]([N:8]([CH2:14][C:15]1[CH:20]=[CH:19][C:18]([C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][C:22]=2[C:27]2[N:31]([C:32]([C:45]3[CH:50]=[CH:49][CH:48]=[CH:47][CH:46]=3)([C:39]3[CH:44]=[CH:43][CH:42]=[CH:41][CH:40]=3)[C:33]3[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=3)[N:30]=[N:29][N:28]=2)=[CH:17][CH:16]=1)[C:9](=[O:13])[CH2:10][CH2:11][CH3:12])[CH:6]=O.N1C=CC=CC=1>O>[OH:3][N:2]=[CH:4][C@@H:5]([N:8]([CH2:14][C:15]1[CH:16]=[CH:17][C:18]([C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][C:22]=2[C:27]2[N:31]([C:32]([C:33]3[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=3)([C:45]3[CH:46]=[CH:47][CH:48]=[CH:49][CH:50]=3)[C:39]3[CH:40]=[CH:41][CH:42]=[CH:43][CH:44]=3)[N:30]=[N:29][N:28]=2)=[CH:19][CH:20]=1)[C:9](=[O:13])[CH2:10][CH2:11][CH3:12])[CH3:6]

Participants

5

Procedure

Hydroxylamine hydrochloride (25.4 mg, 0.4 mmol) was added to a solution of intermediate (5c) (174 mg, 0.3 mmol), pyridine (3 mL, 37 mmol) and water (1.5 mL, 83 mmol) at room temperature. After 15 minutes, water (10 mL) was added and the mixture was extracted with EtOAc (3×20 mL). The combined organic extracts were washed with saturated aqueous NaCl (10 mL), dried over MgSO4, filtered, and concentrated in vacuo. Silica gel chromatography gave intermediate (5d) as a white solid (148 mg).

Workup

  1. extractionthe mixture was extracted with EtOAc (3×20 mL)
  2. washThe combined organic extracts were washed with saturated aqueous NaCl (10 mL)
  3. dry with materialdried over MgSO4
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-1b9679fc8bad4999a6dbcdb3dd4789c9
Source dataset
uspto-grants-2013_03
Patent number
US08394846B2

Reaction notes

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