Hydrochloric Acid → HCID 86739033, compound
Reaction equation
C(O[C:6]([N:8](C)[CH2:9][C@H:10]([OH:19])[C@@H:11]([OH:18])[C@H:12]([OH:17])[C:13](=[O:16])[CH2:14][OH:15])=O)(C)(C)C.[ClH:21]>>[ClH:21].[CH3:6][NH:8][CH2:9][C@H:10]([OH:19])[C@@H:11]([OH:18])[C@H:12]([OH:17])[C:13](=[O:16])[CH2:14][OH:15]Participants
3
Procedure
8 g (0.027 mole) of N-tert.-butoxycarbonyl-6-methylamino-6-desoxy-L-sorbose were deblocked hydrolytically in a manner analogous to that in Example 9. 5 g of the syrupy hydrochloride, which was immediately further processed because of its readiness to decompose, were obtained.
Workup
- customwere obtained
Sources & evidence
- ORD record
- ord-7782ae5a696d4162bcc1e199664826e2
- Source dataset
- uspto-grants-1983_09
- Patent number
- US04405714
Reaction notes
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