Methane → HCID 58092731, compound

HRID 1807685Notes

Reaction equation

HRID 1807685 reaction equation
[NH4+:1].[Cl-].[CH4:3].C[O:5][C:6]([C@@H:8]1[C@H:12]([CH2:13][N:14]2[CH2:19][CH2:18][O:17][CH2:16][CH2:15]2)[CH2:11][CH2:10][N:9]1[C@H](C1C=CC=CC=1)C)=O.[C:28]1([CH3:34])[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1>C[Al](C)C>[N:14]1([CH2:13][C@@H:12]2[CH2:11][CH2:10][N:9]([C@H:34]([C:28]3[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=3)[CH3:3])[C@@H:8]2[C:6]([NH2:1])=[O:5])[CH2:19][CH2:18][O:17][CH2:16][CH2:15]1

Participants

6

Procedure

Trimethylaluminum in toluene (2 M, 2.89 mmol) was added dropwise to a mixture of NH4Cl (2.89 mmol) in toluene (3 mL) at 0° C. with the formation of methane gas. The reaction mixture was allowed to warm to rt, stirred for a further 15 min and then slowly treated with a solution of (2S,3S)-3-morpholin-4-ylmethyl-1-((S)-1-phenyl-ethyl)-pyrrolidine-2-carboxylic acid methyl ester (Stage 37.3) (1.444 mmol) in toluene (9 mL). Additional reagent prepared from NH4Cl (2.89 mmol) in toluene (2 mL) and trimethylaluminum in toluene (2 M, 2.89 mmol) at 0° C. was added after 18 h. After stirring for 60 h, the mixture was cooled to 0° C., quenched with 1M HCl and then washed with CH2Cl2 (3×). The aqueous phase was basified with a 1:1 saturated solution of NaHCO3/saturated solution of Rochelle's salt and extracted with THF (10×). The combined organic layers were dried (Na2SO4), filtered and concentrated. The residue was purified by silica gel column chromatography to afford the title compound as a yellow oil. HPLC: tR=2.18 min (method G); ESI-MS: [M+H]+ 318.

Workup

  1. additionwas added after 18 h
  2. stirringAfter stirring for 60 h
  3. temperaturethe mixture was cooled to 0° C.
  4. customquenched with 1M HCl
  5. washwashed with CH2Cl2 (3×)
  6. extractionextracted with THF (10×)
  7. dry with materialThe combined organic layers were dried (Na2SO4)
  8. filtrationfiltered
  9. concentrationconcentrated
  10. customThe residue was purified by silica gel column chromatography

Sources & evidence

ORD record
ord-32098a0894b34c5781052e38faecae14
Source dataset
uspto-grants-2013_01
Patent number
US08357707B2

Reaction notes

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