HCID 22056681, compound → HCID 25234505, compound

HRID 1641020Notes

Reaction equation

HRID 1641020 reaction equation
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[C:3]([C:10]([O:12][CH2:13][C:14]23C[CH2:20][N:17]([CH2:18][CH2:19]2)[CH2:16][CH2:15]3)=[O:11])=[CH:2]1.N12CC([CH2:29][OH:30])(CC1)CC2>>[CH3:29][O:30][C:6]1[CH:5]=[C:4]2[C:9](=[CH:8][CH:7]=1)[NH:1][CH:2]=[C:3]2[C:10]([O:12][CH2:13][C:14]12[CH2:20][N:17]([CH2:16][CH2:15]1)[CH2:18][CH2:19]2)=[O:11]

Participants

3

Reactant 2

HCID 22056681HCID 22056681, compoundHCID 25234267(Quinuclidin-4-yl)methyl 1H-indole-3-carboxylate

Product 1

HCID 25234505HCID 25234505, compound

Procedure

1-Azabicyclo[2.2.1]heptan-4-ylmethyl 5-methoxy-1H-indole-3-carboxylate was synthesized using the procedure described for (Quinuclidin-4-yl)methyl 1H-indole-3-carboxylate using 1-Azabicyclo[2.2.1]heptan-4-ylmethanol. MS: (m/e) 300.

Sources & evidence

ORD record
ord-cb600ad8fb3c46558da06c545ccf05d2
Source dataset
uspto-grants-2012_02
Patent number
US08114891B2

Reaction notes

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