HCID 22056681, compound → HCID 25234434, compound

HRID 1641019Notes

Reaction equation

HRID 1641019 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]23[CH2:21]C[N:17]([CH2:18][CH2:19]2)[CH2:16][CH2:15]3)=[O:11])=[CH:2]1.N12CC(CO)(CC1)CC2>>[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]23[CH2:21][N:17]([CH2:18][CH2:19]2)[CH2:16][CH2:15]3)=[O:11])=[CH:2]1

Participants

3

Reactant 2

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

Product 1

HCID 25234434HCID 25234434, compound

Procedure

1-Azabicyclo[2.2.1]heptan-4-ylmethyl 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) 270.

Sources & evidence

ORD record
ord-fa7fba66d3f44a91968abf02c13bcb2c
Source dataset
uspto-grants-2012_02
Patent number
US08114891B2

Reaction notes

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