Water → HCID 67170495, compound

HRID 2168036Notes

Reaction equation

HRID 2168036 reaction equation
[C@H:1]12[CH2:7][C@H:4]([CH:5]=[CH:6]1)[CH2:3][CH:2]2[CH2:8][O:9][C:10]1[CH:15]=[CH:14][C:13]([S:16]([NH2:19])(=[O:18])=[O:17])=[CH:12][C:11]=1[N+:20]([O-:22])=[O:21].C[N+]1([O-])CC[O:27]CC1.[OH2:31]>O1CCCC1.O=[Os](=O)(=O)=O>[OH:31][C@H:5]1[C@@H:6]([OH:27])[C@@H:1]2[CH2:7][C@H:4]1[CH2:3][CH:2]2[CH2:8][O:9][C:10]1[CH:15]=[CH:14][C:13]([S:16]([NH2:19])(=[O:18])=[O:17])=[CH:12][C:11]=1[N+:20]([O-:22])=[O:21]

Participants

6

Reactant 3

HCID 962WaterHCID 82029Methyl morpholine oxideHCID 67169824HCID 67169824, compound

Product 1

HCID 67170495HCID 67170495, compound

Reagents, catalysts & solvents 2

HCID 30318Osmium TetroxideCatalystHCID 8028TetrahydrofuranSolvent

Procedure

To a solution of EXAMPLE 201A (340 mg) in tetrahydrofuran (10 mL) and water (1 mL) was added N-methylmorpholine N-oxide (184 mg) and OsO4 (2.5% in 2-methyl-2-propanol) (1.05 mL). The reaction mixture was stirred overnight and purified by reverse phase HPLC to provide two isomers, which were temporarily assigned as EXAMPLE 203A and EXAMPLE 203B, respectively.

Workup

  1. custompurified by reverse phase HPLC
  2. customto provide two isomers, which

Sources & evidence

ORD record
ord-d74277a0cf344da69e510e3cb457f43a
Source dataset
uspto-grants-2015_06
Patent number
US09045475B2

Reaction notes

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