Water → 5-Bromo-1-methyl-3-(5-(3-(oxetan-3-yl)-3,8-diazabicyclo[3.2.1]octan-8-yl)pyridin-2-ylamino)pyridine-2(1H)-one

HRID 1021758Notes

Reaction equation

[CH:1]12[N:8]([C:9]3[CH:10]=[CH:11][C:12]([NH:15][C:16]4[C:17](=[O:24])[N:18]([CH3:23])[CH:19]=[C:20]([Br:22])[CH:21]=4)=[N:13][CH:14]=3)[CH:5]([CH2:6][CH2:7]1)[CH2:4][NH:3][CH2:2]2.[O:25]1[CH2:28][C:27](=O)[CH2:26]1.[BH3-]C#N.[Na+].O>CO.[Cl-].[Zn+2].[Cl-]>[Br:22][C:20]1[CH:21]=[C:16]([NH:15][C:12]2[CH:11]=[CH:10][C:9]([N:8]3[CH:5]4[CH2:6][CH2:7][CH:1]3[CH2:2][N:3]([CH:27]3[CH2:28][O:25][CH2:26]3)[CH2:4]4)=[CH:14][N:13]=2)[C:17](=[O:24])[N:18]([CH3:23])[CH:19]=1

Participants

Conditions

Temperature: 50 °C

Procedure

A mixture of 152d (676 mg, 1.7 mmol), oxetan-3-one (251 mg, 3.5 mmol), NaBH3CN (274 mg, 4.4 mmol), and zinc chloride (592 mg, 4.4 mmol) in methanol (30 mL) was stirred at 50° C. for 5 hours. water was added and the mixture was concentrated under reduced pressure. The residue was extracted with dichloromethane three times. The combined extract was concentrated under reduced pressure to afford crude 152e as a yellow solid (650 mg, 84%), which was used in the next step without further purification. MS-ESI: [M+H]+ 446.2.

Workup

concentrationthe mixture was concentrated under reduced pressure
extractionThe residue was extracted with dichloromethane three times
extractionThe combined extract
concentrationwas concentrated under reduced pressure

Sources & evidence

ORD record: ord-04a2af11a9364d409966a2f520439210
Source dataset: uspto-grants-2014_05
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08716274B2

Reaction notes

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