Methoxymethyl-triphenylphosphonium chloride → HCID 67148474, compound

HRID 2234100Notes

Reaction equation

[Cl-].[CH3:2][O:3][CH2:4][P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.[CH2:24]([Li])CCC.[C:29]([O:33][C:34]([N:36]1[C:44]2[C:39](=[CH:40][CH:41]=[C:42](C=O)[CH:43]=2)[CH:38]=[C:37]1[C:47]1[CH:52]=[C:51]([C:53]2[CH:58]=[CH:57][N:56]=[CH:55][CH:54]=2)[N:50]=[N:49][C:48]=1[O:59][CH3:60])=[O:35])([CH3:32])([CH3:31])[CH3:30]>C1COCC1>[C:29]([O:33][C:34]([N:36]1[C:44]2[C:39](=[CH:40][CH:41]=[C:42]([CH:24]=[CH:4][O:3][CH3:2])[CH:43]=2)[CH:38]=[C:37]1[C:47]1[CH:52]=[C:51]([C:53]2[CH:58]=[CH:57][N:56]=[CH:55][CH:54]=2)[N:50]=[N:49][C:48]=1[O:59][CH3:60])=[O:35])([CH3:31])([CH3:30])[CH3:32]

Participants

Conditions

Temperature: -78 °C

Procedure

1.23 g Methoxymethyltriphenylphoshonium chloride is suspended in 10 mL THF and cooled to −78° C. 2.20 mL butyllithium (1.6 M in hexanes) is added dropwise and the resulting mixture is stirred for 30 min at −78° C. and then warmed in an ice bath to 0° C. After addition of a solution of 734 mg 6-formyl-2-(3-methoxy-6-pyridin-4-yl-pyridazin-4-yl)-indole-1-carboxylic acid tert-butyl ester (see above) in 5 mL THF the reaction mixture is heated to reflux for 5 hours. After cooling to rt, the reaction mixture is diluted with heptanes, washed with water, dried (MgSO4) and concentrated in vacuo. The resulting 280 mg crude enol ether is directly used in the next step.

Workup

temperaturewarmed in an ice bath to 0° C
temperatureis heated
temperatureto reflux for 5 hours
temperatureAfter cooling to rt
washwashed with water
dry with materialdried (MgSO4)
concentrationconcentrated in vacuo

Sources & evidence

ORD record: ord-f6a2c84b44274a60985f0b3678dd1b76
Source dataset: uspto-grants-2010_05
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07709466B2

Reaction notes

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