2-n-Butylthiophene → HCID 11462929, compound

HRID 1434943Notes

Reaction equation

HRID 1434943 reaction equation
Cl[C:2]1[CH:7]=[CH:6][N:5]=[C:4]([NH:8][CH:9]2[CH2:14][C:13]([CH3:16])([CH3:15])[NH:12][C:11]([CH3:18])([CH3:17])[CH2:10]2)[N:3]=1.[CH2:19]([C:23]1[S:24][CH:25]=[CH:26][CH:27]=1)[CH2:20][CH2:21][CH3:22]>>[CH2:19]([C:23]1[S:24][C:25]([C:2]2[CH:7]=[CH:6][N:5]=[C:4]([NH:8][CH:9]3[CH2:14][C:13]([CH3:16])([CH3:15])[NH:12][C:11]([CH3:18])([CH3:17])[CH2:10]3)[N:3]=2)=[CH:26][CH:27]=1)[CH2:20][CH2:21][CH3:22]

Participants

3

Procedure

The title compound was prepared analogous to Method C, starting from (4-chloro-pyrimidin-2-yl)-(2,2,6,6-tetramethyl-piperidin-4-yl)-amine and 2-butyl-thiophene.

Sources & evidence

ORD record
ord-bbe568e957b54510b77bccdda66054b8
Source dataset
uspto-grants-2009_11
Patent number
US07615562B2

Reaction notes

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