Hydrochloric Acid → HCID 68612180, compound
Reaction equation
[ClH:1].C(OC([N:9]1[CH2:12][CH2:11][C@H:10]1[CH2:13][O:14][C:15]1[CH:16]=[C:17]([CH2:21][C@@H:22]2[CH2:24][C@H:23]2[CH2:25][OH:26])[CH:18]=[N:19][CH:20]=1)=O)(C)(C)C>CCOCC.CO>[ClH:1].[NH:9]1[CH2:12][CH2:11][C@H:10]1[CH2:13][O:14][C:15]1[CH:16]=[C:17]([CH2:21][C@@H:22]2[CH2:24][C@H:23]2[CH2:25][OH:26])[CH:18]=[N:19][CH:20]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
2M anhydrous HCl in ether is added to a stirred solution of (1R,2S)-2-[[5-[[1-(tert-butoxycarbonyl)-2(S)-azetidinyl]methoxy]-3-pyridyl]methyl]cyclopropylmethanol in dry MeOH at 0° C. The mixture is stirred at room temperature overnight and the conversion of starting material confirmed by TLC. The above solution is concentrated and purified by HPLC to obtain the title compound.
Workup
- concentrationThe above solution is concentrated
- custompurified by HPLC
Sources & evidence
- ORD record
- ord-af6f5f5f88dc4c7683c2c7739c654ced
- Source dataset
- uspto-grants-2013_05
- Patent number
- US08445684B2
Reaction notes
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