Cesium carbonate → HCID 86635291, compound

HRID 250072

Reaction equation

HRID 250072 reaction equation
[ClH:1].Cl.[NH2:3][CH2:4][C@@:5]1([OH:13])[CH:10]2[CH2:11][CH2:12][N:7]([CH2:8][CH2:9]2)[CH2:6]1.C([O-])([O-])=O.[Cs+].[Cs+].N([C:23]1C=[C:27]([C:29]2C=NC=CC=2)[N:26]=[CH:25][N:24]=1)=C=S.C(N=C=[N:40][CH:41](C)C)(C)C>CN(C)C=O>[Cl:1][C:29]1[N:40]=[CH:41][C:25]([NH:24][C:23]2[O:13][C@@:5]3([CH2:4][N:3]=2)[CH:10]2[CH2:9][CH2:8][N:7]([CH2:12][CH2:11]2)[CH2:6]3)=[N:26][CH:27]=1

Participants

6

Procedure

To (S)-3-(aminomethyl)quinuclidin-3-ol dihydrochloride (0.13 g, 0.560 mmol) in N,N-dimethylformamide (20 mL) was added Cs2CO3 (0.46 g, 1.4 mmol) and 4-isothiocyanato-6-(pyridin-3-yl)pyrimidine (0.12 g, 0.56 mmol). The suspension was stirred at room temperature for 30 minutes. N,N′-Diisopropylcarbodiimide (0.26 mL, 1.7 mmol) was then added and the mixture was stirred at room temperature for 18 hours. The mixture was concentrated and purified by silica gel chromatography (0-10% [9:1 methanol:ammonium hydroxide]-ethyl acetate) to afford (S)—N-(5-chloropyrazin-2-yl)-4H-1′-azaspiro[oxazole-5,3′-bicyclo[2.2.2]octan]-2-amine (0.182 g, 0.613 mmol, 35% yield) as an off-white solid. 1H NMR (400 MHz, MeOD) δ ppm 9.13-9.21 (1 H, m), 8.82 (1 H, d), 8.63 (1 H, dd), 8.44 (1 H, dt), 7.56 (1 H, dd), 7.31 (1 H, s), 4.06 (1 H, d), 3.76 (1 H, d), 3.20-3.28 (1 H, m), 3.08-3.16 (1 H, m), 2.72-3.01 (4 H, m), 2.00-2.24 (2 H, m), 1.52-1.83 (3 H, m). LCMS R.T.=0.72; [M+H]+=337.2.

Workup

  1. stirringthe mixture was stirred at room temperature for 18 hours
  2. concentrationThe mixture was concentrated
  3. custompurified by silica gel chromatography (0-10% [9:1 methanol:ammonium hydroxide]-ethyl acetate)

Sources & evidence

ORD record
ord-fed4bc22ade541e4899babdf397d8077
Source dataset
uspto-grants-2011_01
Patent number
US07863291B2

Linked notes

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