Ammonium Chloride → HCID 59135975, compound

HRID 2239150Notes

Reaction equation

HRID 2239150 reaction equation
[CH3:1][N:2]([S:27]([C:30]1[S:31][CH:32]=[CH:33][CH:34]=1)(=[O:29])=[O:28])[C:3]1[CH:4]=[CH:5][CH:6]=[C:7]2[C:11]=1[NH:10][C:9]([C:12]1[S:13][C:14]3([CH2:21][CH2:20][N:19]([CH2:22]C(OC)=O)[CH2:18][CH2:17]3)[CH2:15][N:16]=1)=[CH:8]2.[CH3:35][Li].C([O:39][CH2:40][CH3:41])C.[Cl-].[NH4+]>O1CCCC1>[OH:39][C:40]([CH3:41])([CH3:35])[CH2:22][N:19]1[CH2:20][CH2:21][C:14]2([S:13][C:12]([C:9]3[NH:10][C:11]4[C:7]([CH:8]=3)=[CH:6][CH:5]=[CH:4][C:3]=4[N:2]([CH3:1])[S:27]([C:30]3[S:31][CH:32]=[CH:33][CH:34]=3)(=[O:29])=[O:28])=[N:16][CH2:15]2)[CH2:17][CH2:18]1

Participants

5

Procedure

To a solution of methyl (2-{7-[methyl(2-thienylsulfonyl)amino]-1H-indol-2-yl}-1-thia-3,8-diazaspiro[4.5]dec-2-en-8-yl)acetate (211 mg) in tetrahydrofuran (3 mL) was added 1.5M methyllithium-diethyl ether solution (2 mL) at room temperature, and the mixture was stirred for 30 min. Saturated aqueous ammonium chloride solution was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4), and concentrated. The obtained residue was subjected to silica gel column chromatography to give the title compound (92 mg, yield 44%) as white crystals from a fraction eluted with ethyl acetate:hexane=1:3. melting point 191° C.

Workup

  1. extractionthe mixture was extracted with ethyl acetate
  2. washThe ethyl acetate layer was washed with saturated brine
  3. dry with materialdried (MgSO4)
  4. concentrationconcentrated

Sources & evidence

ORD record
ord-95ef0752b3124e94886b167f1fd1f6f0
Source dataset
uspto-grants-2010_05
Patent number
US07718798B2

Reaction notes

Loading…