Acetaldehyde → HCID 58062354, compound

HRID 1039645Notes

Reaction equation

HRID 1039645 reaction equation
[CH3:1][N:2]([C@H:16]1[CH2:24][C:23]2[C:18](=[CH:19][CH:20]=[C:21]([CH:25]3[CH2:29][CH2:28][CH2:27][NH:26]3)[CH:22]=2)[CH2:17]1)[C:3]([C:5]1[CH:10]=[CH:9][C:8]([O:11][CH2:12][CH:13]2[CH2:15][CH2:14]2)=[CH:7][N:6]=1)=[O:4].[CH:30](=O)[CH3:31]>>[CH2:30]([N:26]1[CH2:27][CH2:28][CH2:29][CH:25]1[C:21]1[CH:22]=[C:23]2[C:18](=[CH:19][CH:20]=1)[CH2:17][C@@H:16]([N:2]([CH3:1])[C:3]([C:5]1[CH:10]=[CH:9][C:8]([O:11][CH2:12][CH:13]3[CH2:14][CH2:15]3)=[CH:7][N:6]=1)=[O:4])[CH2:24]2)[CH3:31]

Participants

3

Reactant 2

HCID 177AcetaldehydeHCID 66680391HCID 66680391, compound

Product 1

HCID 58062354HCID 58062354, compound

Procedure

According to method A, N-methyl-N-((R)-5-pyrrolidin-2-ylindan-2-yl)-5-cyclopropylmethoxypyridine-2-carboxamide was reacted with acetaldehyde. The product was thus obtained with the monoisotopic molecular weight of 419.26 (C26H33N3O2); MS (ESI): 420.4 (M+H+).

Workup

  1. customThe product was thus obtained with the monoisotopic molecular weight of 419.26 (C26H33N3O2)

Sources & evidence

ORD record
ord-1ea4cb56c31a436b9112a1ccb49a1e30
Source dataset
uspto-grants-2013_10
Patent number
US08552199B2

Reaction notes

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