Hydrochloric Acid → HCID 67315126, compound
Reaction equation
C[O:2][C:3]([CH:5]1[N:9](C(OC(C)(C)C)=O)[CH2:8][CH:7]([N:17]2[CH2:21][CH2:20][CH2:19][CH2:18]2)[CH2:6]1)=O.[H-].[Al+3].[Li+].[H-].[H-].[H-].[ClH:28]>O1CCOCC1>[ClH:28].[ClH:28].[N:17]1([C@H:7]2[CH2:6][C@@H:5]([CH2:3][OH:2])[NH:9][CH2:8]2)[CH2:18][CH2:19][CH2:20][CH2:21]1Participants
5
Procedure
The title compound was prepared in analogy to 193B, by reduction of 3′S,5′S)-[1,3′]Bipyrrolidinyl-1′,5′-dicarboxylic acid 1′-tert-butyl ester 5′-methyl ester with lithium aluminium hydride and subsequent deprotection with 4M hydrochloric acid in dioxane. MS: 171.3 (MH+).
Sources & evidence
- ORD record
- ord-5cddac67714a401a9b26586084fd352a
- Source dataset
- uspto-grants-2011_07
- Patent number
- US07977358B2
Reaction notes
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