N-Methylfurfurylamine → HCID 58808683, compound

HRID 1921442Notes

Reaction equation

HRID 1921442 reaction equation
[CH2:1]([C:3]1[C:8](=[O:9])[NH:7][C:6]([CH3:10])=[C:5]([C:11]2[S:15][C:14]([S:16](Cl)(=[O:18])=[O:17])=[CH:13][CH:12]=2)[CH:4]=1)[CH3:2].[O:20]1[CH:24]=[CH:23][CH:22]=[C:21]1[CH2:25][NH:26][CH3:27]>>[O:20]1[CH:24]=[CH:23][CH:22]=[C:21]1[CH2:25][N:26]([CH3:27])[S:16]([C:14]1[S:15][C:11]([C:5]2[CH:4]=[C:3]([CH2:1][CH3:2])[C:8](=[O:9])[NH:7][C:6]=2[CH3:10])=[CH:12][CH:13]=1)(=[O:18])=[O:17]

Participants

3

Reactant 2

HCID 78492N-MethylfurfurylamineHCID 866103525-(5-Ethyl-2-methyl-6-oxo-1,6-dihydropyridin-3-yl)thiophene-2-sulfonyl chloride

Product 1

HCID 58808683HCID 58808683, compoundYield 78%

Procedure

5-(5-Ethyl-2-methyl-6-oxo-1,6-dihydropyridin-3-yl)thiophene-2-sulfonyl chloride is reacted with furan-2-ylmethyl-methyl-amine as described in Step 5, Example 24 to give the title compound as a cream solid (78% yield). LC/MS: RT 3.03 min, n/e 393 (M+H); 1H NMR (δ, ppm): 11.85 (1H, s), 7.62 (2H, m), 7.35 (1H, s), 7.23 (1H, d), 6.40 (2H, dd), 4.27 (2H, s), 2.70 (3H, s), 2.41 (2H, q), 2.32 (3H, s), 1.10 (3H, t).

Sources & evidence

ORD record
ord-98ba8913638b4145a1c7f04d392bd9d8
Source dataset
uspto-grants-2012_05
Patent number
US08173682B2

Reaction notes

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