4-Methylmorpholine → HCID 70561849, compound

HRID 1427306Notes

Reaction equation

HRID 1427306 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([N:13]2[C:21]3[CH:20]=[CH:19][CH:18]=[C:17]([NH2:22])[C:16]=3[CH:15]=[CH:14]2)([CH2:11][CH3:12])[CH2:9][CH3:10])=[CH:4][CH:3]=1.CN1CCOCC1.[CH3:30][S:31](Cl)(=[O:33])=[O:32]>ClCCl.O>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]([N:13]2[C:21]3[C:16](=[C:17]([NH:22][S:31]([CH3:30])(=[O:33])=[O:32])[CH:18]=[CH:19][CH:20]=3)[CH:15]=[CH:14]2)([CH2:11][CH3:12])[CH2:9][CH3:10])=[CH:6][CH:7]=1

Participants

6

Reactant 3

HCID 79724-MethylmorpholineHCID 31297Methanesulfonyl chlorideHCID 70562044HCID 70562044, compound

Product 1

HCID 70561849HCID 70561849, compound

Reagents, catalysts & solvents 2

HCID 962WaterSolventHCID 6344DichloromethaneSolvent

Procedure

To a solution of the product of Step B (50 mg, 0.16 mmol) and N-methylmorpholine (32 mg, 0.32 mmol) in dichloromethane (2 mL) was added methanesulfonyl chloride (23 mg, 0.24 mmol) at room temperature. The mixture was stirred for 2 h, then diluted with water (15 mL) and extracted with ethyl acetate. The combined organic layers were washed with brine (10 mL), dried over Na2SO4, filtered and concentrated. The crude product was purified by PREP-TLC eluting with PE/EA (2/1, v/v) to give the title compound as a colorless solid. LC/MS m/z=391.0[M+H]+.

Workup

  1. extractionextracted with ethyl acetate
  2. washThe combined organic layers were washed with brine (10 mL)
  3. dry with materialdried over Na2SO4
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customThe crude product was purified
  7. washby PREP-TLC eluting with PE/EA (2/1

Sources & evidence

ORD record
ord-2de7958c0c324b2381b466bd988ae8d3
Source dataset
uspto-grants-2015_01
Patent number
US08933113B2

Reaction notes

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