Methyl Isocyanate → HCID 18545964, compound

HRID 1385080Notes

Reaction equation

HRID 1385080 reaction equation
[Cl:1][C:2]1[CH:10]=[C:9]2[C:5]([C:6]([C:11]3[CH2:12][CH2:13][N:14]([CH2:17][CH2:18][CH:19]4[C:27]5[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=5)[NH:21][CH2:20]4)[CH2:15][CH:16]=3)=[CH:7][NH:8]2)=[CH:4][CH:3]=1.[C:28]([O-:33])(=[O:32])[C:29]([O-:31])=[O:30].[CH3:34][N:35]=[C:36]=[O:37]>ClCCl>[C:28]([OH:33])(=[O:32])[C:29]([OH:31])=[O:30].[Cl:1][C:2]1[CH:10]=[C:9]2[C:5]([C:6]([C:11]3[CH2:12][CH2:13][N:14]([CH2:17][CH2:18][CH:19]4[C:27]5[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=5)[N:21]([C:36]([NH:35][CH3:34])=[O:37])[CH2:20]4)[CH2:15][CH:16]=3)=[CH:7][NH:8]2)=[CH:4][CH:3]=1

Participants

5

Procedure

To a solution of 6-chloro-3-[1-[2-(2,3-dihydro-1H-indol-3-yl)ethyl]-1,2,3,6-tetrahydropyridin-4-yl]-1H-indole, oxalate 30a, as the free base, (3.6 g) in dichloromethane (100 ml) was added methylisocyanate (1.4 g) in dichloromethane (20 ml). The mixture was stirred at room temperature for 16 h, and the solvent was removed in vacuo. The residue was purified on silica gel eluted with ethyl acetate-ethanol-triethylamine (90:10:5) to give the crude product, which was recrystallized (methanol-ethyl acetate-ether) to give the title compound (1.8 g). 1H NMR (DMSO-d6) δ 1.60-1.70 (m, 1H), 1.95-2.05 (m, 1H), 2.40-2.60 (m, 4H), 2.60-2.75 (m, 5H), 3.15 (q, 2H), 3.35-3.50 (m, 1H), 3.55-3.65 (m, 1H), 4.00 (t, 1H), 6.10 (broad s, 1H), 6.55 (d, 1H), 6.85 (t, 1H), 7.05 (d, 1H), 7.10 (t, 1H), 7.20 (d, 1H), 7.45 (s, 2H), 7.80 (d, 1H), 7.85 (d, 1H), 11.25 (broad s, 1H). MS m/z (%): 437, 435 (MH+, 2%, 6%), 201 (54%), 189 (100%), 144 (64%).

Workup

  1. customthe solvent was removed in vacuo
  2. customThe residue was purified on silica gel
  3. washeluted with ethyl acetate-ethanol-triethylamine (90:10:5)
  4. customto give the crude product, which
  5. customwas recrystallized (methanol-ethyl acetate-ether)

Sources & evidence

ORD record
ord-1ccb6362686b46b2a822012ed04866c8
Source dataset
uspto-grants-2001_07
Patent number
US06262087B1

Reaction notes

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