Hydrochloric Acid → HCID 67220395, compound

HRID 1798918Notes

Reaction equation

HRID 1798918 reaction equation
[F:1][C:2]1[C:24]([CH3:25])=[CH:23][C:5]2[N:6]([CH:10]3[CH2:15][CH2:14][N:13](C(OC(C)(C)C)=O)[CH2:12][CH2:11]3)[C:7](=[O:9])[O:8][C:4]=2[CH:3]=1.Cl>ClCCl.CO.ClCCl>[F:1][C:2]1[C:24]([CH3:25])=[CH:23][C:5]2[N:6]([CH:10]3[CH2:11][CH2:12][NH:13][CH2:14][CH2:15]3)[C:7](=[O:9])[O:8][C:4]=2[CH:3]=1

Participants

5

Reactant 2

HCID 313Hydrochloric AcidHCID 58287304HCID 58287304, compound

Product 1

HCID 67220395HCID 67220395, compoundYield 111.5%

Reagents, catalysts & solvents 2

HCID 6344DichloromethaneSolventHCID 21226129Dichloromethane methanolSolvent

Procedure

1,1-Dimethylethyl 4-(6-fluoro-5-methyl-2-oxo-1,3-benzoxazol-3(2H)-yl)-1-piperidine carboxylate (D2, 546 mg, 1.14 mmol) was dissolved in dichloromethane (10 mL) at rt. HCl (10 mL, 40 mmol, 4 M in 1,4-dioxane) was added and the reaction was stirred overnight. It was then concentrated by rotary evaporation to give a pale brown solid. The residue was dissolved in methanol/dichloromethane and purified by SCX (5 g, eluting with methanol, followed by 2 M ammonia in methanol). The ammonia/methanol fraction was concentrated by rotary evaporation to give 6-fluoro-5-methyl-3-(4-piperidinyl)-1,3-benzoxazol-2(3H)-one (D3, 318 mg, 72% purity, 80% yield) as an orange oil.

Workup

  1. concentrationIt was then concentrated by rotary evaporation
  2. customto give a pale brown solid
  3. custompurified by SCX (5 g, eluting with methanol, followed by 2 M ammonia in methanol)
  4. concentrationThe ammonia/methanol fraction was concentrated by rotary evaporation

Sources & evidence

ORD record
ord-08d60e7207254ae18fdd8aeef45d5b79
Source dataset
uspto-grants-2013_01
Patent number
US08344000B2

Reaction notes

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