2-Chloro-6-methylbenzothiazole → HCID 67520591, compound

HRID 1926380Notes

Reaction equation

HRID 1926380 reaction equation
F[C:2]1[CH:28]=[CH:27][C:5]2[N:6]=[C:7]([C:9]3[C:10]([NH2:26])=[N:11][CH:12]=[C:13]([C:15]4[CH:16]=[N:17][N:18]([CH:20]5[CH2:25][CH2:24][NH:23][CH2:22][CH2:21]5)[CH:19]=4)[CH:14]=3)[S:8][C:4]=2[CH:3]=1.Cl[C:30]1SC2C=C(C)C=CC=2N=1>>[CH3:30][C:2]1[CH:28]=[CH:27][C:5]2[N:6]=[C:7]([C:9]3[C:10]([NH2:26])=[N:11][CH:12]=[C:13]([C:15]4[CH:16]=[N:17][N:18]([CH:20]5[CH2:25][CH2:24][NH:23][CH2:22][CH2:21]5)[CH:19]=4)[CH:14]=3)[S:8][C:4]=2[CH:3]=1

Participants

3

Reactant 2

HCID 20498662-Chloro-6-methylbenzothiazoleHCID 675210153-(6-fluorobenzothiazol-2-yl)-5-(1-piperidin-4-yl-1H-pyrazol-4-yl)-pyridin-2-ylamine

Product 1

HCID 67520591HCID 67520591, compound

Procedure

Same procedure as 3-(6-fluorobenzothiazol-2-yl)-5-(1-piperidin-4-yl-1H-pyrazol-4-yl)-pyridin-2-ylamine except using 2-chloro-6-methyl-1,3-benzothiazole in place of 2-chloro-6-fluorobenzothiazole to afford the title compound as a yellow solid. 1H NMR (400 MHz, DMSO-d6): δ=2.10-2.31 (m, 4H), 3.12 (q, J=10.6 Hz, 2H), 3.42 (d, J=12.4 Hz, 2H), 4.47-4.57 (m, 1H), 7.41 (d, J=6.9 Hz, 1H), 7.96-8.02 (m, 2H), 8.05 (s, 1H), 8.31 (br. s., 1H), 8.38 (s, 1H), 8.49 (d, J=2.2 Hz, 1H). MS (ES+): m/z=391.15 [MH+]. HPLC: tR=2.22 min (ZQ2, polar—5 min).

Sources & evidence

ORD record
ord-274776aa77f54e9cb8f842b716c816ba
Source dataset
uspto-grants-2012_05
Patent number
US08178668B2

Reaction notes

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