HCID 59532380, compound → HCID 59532367, compound

HRID 2037504Notes

Reaction equation

HRID 2037504 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:13]=[CH:12][C:11]([C@@H:14]([N:16]3[CH2:21][CH2:20][C@:19]([CH2:27][C:28](O)=[O:29])([C:22]4[S:23][CH:24]=[CH:25][CH:26]=4)[O:18][C:17]3=[O:31])[CH3:15])=[CH:10][CH:9]=2)=[CH:4][CH:3]=1>C1COCC1>[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:9]=[CH:10][C:11]([C@@H:14]([N:16]3[CH2:21][CH2:20][C@:19]([CH2:27][CH2:28][OH:29])([C:22]4[S:23][CH:24]=[CH:25][CH:26]=4)[O:18][C:17]3=[O:31])[CH3:15])=[CH:12][CH:13]=2)=[CH:4][CH:3]=1

Participants

3

Procedure

A solution of 2-((S)-3-((S)-1-(4′-fluorobiphenyl-4-yl)ethyl)-2-oxo-6-(thiophen-2-yl)-1,3-oxazinan-6-yl)acetic acid (218 mg, 0.5 mmol) in THF anhydrous (10 mL) was added BH3 (3.0 mL) at 0□ and then stirred at reflux for 2 h. Then the reaction mixture quenched by water and separated, extracted with EtOAc twice. The organic phases was dried over Na2SO4, filtered and concentrated to afford the residue, which was purified by TLC to give (S)-3-((S)-1-(4′-fluorobiphenyl-4-yl)ethyl)-6-(2-hydroxyethyl)-6-(thiophen-2-yl)-1,3-oxazinan-2-one (85 mg, 40%). LC-MS Method 3 tR=1.35, min, m/z=426, 448; 1H NMR (CD3OD): 1.50 (m, 3H), 2.15 (m, 2H), 2.30 (m, 1H), 2.40 (m, 1H), 2.60 (m, 1H), 3.15 (m, 1H), 3.45 (m, 1H), 3.70 (m, 1H), 5.60 (m, 1H), 6.90 (m, 1H), 7.00 (m, 1H), 7.10 (m, 4H), 7.35 (m, 3H), 7.55 (m, 2H).

Workup

  1. temperatureat reflux for 2 h
  2. customThen the reaction mixture quenched by water
  3. customseparated
  4. extractionextracted with EtOAc twice
  5. dry with materialThe organic phases was dried over Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customto afford the residue, which
  9. customwas purified by TLC

Sources & evidence

ORD record
ord-234feea8f9e04bb7a559225ef3c9d2c3
Source dataset
uspto-grants-2013_11
Patent number
US08575156B2

Reaction notes

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