Butylamine → HCID 67314835, compound

HRID 2179699Notes

Reaction equation

HRID 2179699 reaction equation
[ClH:1].[N:2]12[CH2:9][CH2:8][CH:5]([CH2:6][CH2:7]1)[C@H:4]([NH:10][C:11]([C:13]1[O:14][C:15]3[C:21]([C:22]4[CH:23]=[C:24]([CH:28]=[CH:29][CH:30]=4)[C:25](O)=[O:26])=[CH:20][CH:19]=[CH:18][C:16]=3[CH:17]=1)=[O:12])[CH2:3]2.[CH2:31]([NH2:35])[CH2:32][CH2:33][CH3:34]>>[ClH:1].[N:2]12[CH2:7][CH2:6][CH:5]([CH2:8][CH2:9]1)[C@H:4]([NH:10][C:11]([C:13]1[O:14][C:15]3[C:21]([C:22]4[CH:30]=[CH:29][CH:28]=[C:24]([C:25]([NH:35][CH2:31][CH2:32][CH2:33][CH3:34])=[O:26])[CH:23]=4)=[CH:20][CH:19]=[CH:18][C:16]=3[CH:17]=1)=[O:12])[CH2:3]2

Participants

3

Reactant 2

HCID 8007ButylamineHCID 67313210HCID 67313210, compound

Product 1

HCID 67314835HCID 67314835, compound

Procedure

50 mg (0.12 mmol) of 3-(2-{[(3S)-1-azabicyclo[2.2.2]oct-3-ylamino]carbonyl}-1-benzofuran-7-yl)benzoic acid hydrochloride (Example 153) and 17.1 mg (0.23 mmol) of n-butylamine are reacted together by general method E. 49.4 mg (87.5% of theory) of the title compound are obtained.

Sources & evidence

ORD record
ord-89be823dd4444492853480f5f9519d59
Source dataset
uspto-grants-2015_06
Patent number
US09067931B2

Reaction notes

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