Nipecotic Acid → HCID 69435544, compound

HRID 1246851Notes

Reaction equation

Cl[C:2]1[CH:7]=[C:6]([C:8]2[CH:13]=[CH:12][C:11]([S:14][C:15]3[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=3[O:21][CH3:22])=[C:10]([C:23]([F:26])([F:25])[F:24])[CH:9]=2)[CH:5]=[CH:4][N:3]=1.OC1CC[NH:30]C1.[NH:33]1[CH2:41][CH2:40][CH2:39][CH:35]([C:36](O)=[O:37])[CH2:34]1>>[CH3:22][O:21][C:16]1[CH:17]=[CH:18][CH:19]=[CH:20][C:15]=1[S:14][C:11]1[CH:12]=[CH:13][C:8]([C:6]2[CH:5]=[CH:4][N:3]=[C:2]([N:33]3[CH2:41][CH2:40][CH2:39][CH:35]([C:36]([NH2:30])=[O:37])[CH2:34]3)[CH:7]=2)=[CH:9][C:10]=1[C:23]([F:26])([F:25])[F:24]

Participants

Reactant 3

HCID 4498Nipecotic Acid

HCID 982104-Hydroxypyrrolidine

HCID 219068092-Chloro-4-(4-(2-methoxy-phenylsulfanyl)-3-trifluoromethyl-phenyl)-pyridine

Product 1

HCID 69435544HCID 69435544, compound

Procedure

The title compound was prepared according to the procedures of Example 38E, substituting compound 76 with compound 96 (0.039 g, 0.0985 mmol) and 3-hydroxypyrrolidine with nipecotic acid. A yellow solid 107 was obtained (0.0283 g, 59%). 1H-NMR (CDCl3, 400 MHz) δ 1.64–1.74 (m, 1H), 1.90–1.98 (m, 1H), 2.06–2.12 (m, 2H), 2.84–2.92 (m, 1H), 3.52–3.59 (m, 1H), 3.72–3.93 (m, 2H), 3.83 (s, 3H), 4.22–4.27 (m, 1H), 6.96 (d, J=5.9 Hz, 1H), 7.00–7.08 (m, 4H), 7.45–7.52 (m, 3H), 7.84 (s, 1H), 8.31 (d, J=6.5 Hz, 1H); MS (APCI) m/z 489 (M+H)+.

Sources & evidence

ORD record: ord-25990771992e4af797f41db5adf8ad82
Source dataset: uspto-grants-2006_10
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07129247B2

Reaction notes

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