2-Chloro-5-trifluoromethyl-(1,3,4)thiadiazole → HCID 86701214, compound

HRID 2406355Notes

Reaction equation

HRID 2406355 reaction equation
[CH3:1][S:2]([N:5]1[CH2:10][CH:9]=[C:8]([C:11]2[CH:12]=[C:13]3[CH2:27][C:18]4([CH2:26][C:20]5([CH2:25][CH2:24][NH:23][CH2:22][CH2:21]5)[CH2:19]4)[O:17][C:14]3=[CH:15][N:16]=2)[CH2:7][CH2:6]1)(=[O:4])=[O:3].Cl[C:29]1[S:30][C:31]([C:34]([F:37])([F:36])[F:35])=[N:32][N:33]=1>>[CH3:1][S:2]([N:5]1[CH2:6][CH:7]=[C:8]([C:11]2[CH:12]=[C:13]3[CH2:27][C:18]4([CH2:19][C:20]5([CH2:21][CH2:22][N:23]([C:29]6[S:30][C:31]([C:34]([F:37])([F:36])[F:35])=[N:32][N:33]=6)[CH2:24][CH2:25]5)[CH2:26]4)[O:17][C:14]3=[CH:15][N:16]=2)[CH2:9][CH2:10]1)(=[O:4])=[O:3]

Participants

3

Reactant 2

HCID 132467892-Chloro-5-trifluoromethyl-(1,3,4)thiadiazoleHCID 867012045-(1-Methanesulfonyl-1,2,3,6-tetrahydro-pyridin-4-yl)-dispiro[2,3-dihydrofuro[2,3-c]pyridine-2,1'-cyclobutane-3',4''-piperidine]

Product 1

HCID 86701214HCID 86701214, compound

Procedure

The title compound is prepared from 5-(1-methanesulfonyl-1,2,3,6-tetrahydro-pyridin-4-yl)-dispiro[2,3-dihydrofuro[2,3-c]pyridine-2,1′-cyclobutane-3′,4″-piperidine] (HCl salt) and 2-chloro-5-trifluoromethyl-[1,3,4]thiadiazole following a procedure analogous to that described for Example 15. LC (method 3): tR=0.93 min; Mass spectrum (ESI+): m/z=542 [M+H]+.

Sources & evidence

ORD record
ord-6308e5ee4f78466696fe38a35d7106f9
Source dataset
uspto-grants-2014_08
Patent number
US08809361B2

Reaction notes

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