Methanol → HCID 59314292, compound

HRID 1047931Notes

Reaction equation

HRID 1047931 reaction equation
C([O:3][C:4]([C:6]1([NH:15][C:16]([C:18]2[C:19]([N:24]3[CH2:29][CH2:28][CH2:27][CH2:26][CH2:25]3)=[N:20][CH:21]=[CH:22][CH:23]=2)=[O:17])[CH2:14][C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[CH2:7]1)=[O:5])C.O1CCOCC1.CO>O>[N:24]1([C:19]2[C:18]([C:16]([NH:15][C:6]3([C:4]([OH:5])=[O:3])[CH2:14][C:13]4[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=4)[CH2:7]3)=[O:17])=[CH:23][CH:22]=[CH:21][N:20]=2)[CH2:29][CH2:28][CH2:27][CH2:26][CH2:25]1

Participants

5

Procedure

A 100 mL round bottom flask which contains 2-[(3,4,5,6-Tetrahydro-2H-[1,2′]bipyridinyl-3′-carbonyl)-amino]-indan-2-carboxylic acid ethyl ester (343, 330 mg, 0.84 mmol) is charged with 1,4-dioxane (4 mL) and MeOH (4 mL). A stirring bar is added and stirring is initiated. After dissolution, water (1.5 mL) is added followed by the LiOH monohydrate (89 mg, 2.12 mmol). After 62 h, tlc analysis (silica, 50% EtOAc/heptanes) indicates that the starting material is completely consumed. Amberlyst highly acidic exchange resin (0.5 g) is added to the reaction flask. The reaction is capped and allowed to stir at ambient temperature. After 38 h, the contents of the flask are filtered through a pad of Celite. The solvent is removed from the filtrate. The residue is reconstituted with iPrOH/toluene (20+20 mL) and the solvent is removed. This process is repeated 1 time. Pumping to constant weight provides 0.3 g of a white solid.

Workup

  1. customA 100 mL round bottom flask which contains
  2. additionA stirring bar is added
  3. additionis added
  4. customis completely consumed
  5. additionAmberlyst highly acidic exchange resin (0.5 g) is added to the reaction flask
  6. customThe reaction is capped
  7. stirringto stir at ambient temperature
  8. waitAfter 38 h
  9. filtrationthe contents of the flask are filtered through a pad of Celite
  10. customThe solvent is removed from the filtrate
  11. customthe solvent is removed

Sources & evidence

ORD record
ord-cf1b2e24ce3c46168a95161e48e81ab9
Source dataset
uspto-grants-2013_10
Patent number
US08569535B2

Reaction notes

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