Hydrochloric Acid → 2-methyl-3-(2-pyrrolidinylmethoxy)pyridine dihydrochloride, (R)-
Reaction equation
[CH3:1][C:2]1[C:7]([O:8][CH2:9][C@H:10]2[CH2:14][CH2:13][CH2:12][NH:11]2)=[CH:6][CH:5]=[CH:4][N:3]=1.[ClH:15].CC1C(OC[C@@H]2CCCN2)=CC=CN=1>CO>[ClH:15].[ClH:15].[CH3:1][C:2]1[C:7]([O:8][CH2:9][C@H:10]2[CH2:14][CH2:13][CH2:12][NH:11]2)=[CH:6][CH:5]=[CH:4][N:3]=1Participants
5
Procedure
The compound of step 35a was treated with HCl and isolated as described in Example 1b to give a white powder. MS and 1H NMR (D2O, 300 Hz) are similar to 17b. Anal. Calc for C11H16N2O.2.00 HCl: C, 48.82; H, 6.84; N, 10.56; Found C, 49.55; H, 6.95; N, 10.52. [α]25D =- 27.01° (c=1, MeOH).
Workup
- customisolated
- customto give a white powder
Sources & evidence
- ORD record
- ord-8a8653ca04884c5fae148a74fb4d1299
- Source dataset
- uspto-grants-1999_09
- Patent number
- US05948793
Reaction notes
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