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Hydrochloric Acid → HCID 67530865, compound

HRID 1880818
Notes
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Reaction equation

HRID 1880818 reaction equation
C(OC(=O)[NH:7][CH2:8][CH2:9][CH2:10][CH2:11][C@H:12]([N:15]([S:20]([C:23]1[CH:28]=[CH:27][C:26]([C:29]#[N:30])=[CH:25][CH:24]=1)(=[O:22])=[O:21])[CH2:16][CH:17]([CH3:19])[CH3:18])[CH2:13][OH:14])(C)(C)C.Cl>CO>[NH2:7][CH2:8][CH2:9][CH2:10][CH2:11][C@H:12]([N:15]([CH2:16][CH:17]([CH3:19])[CH3:18])[S:20]([C:23]1[CH:24]=[CH:25][C:26]([C:29]#[N:30])=[CH:27][CH:28]=1)(=[O:22])=[O:21])[CH2:13][OH:14]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 313Hydrochloric AcidHCID 57687747HCID 57687747, compound

Product 1

HCID 67530865HCID 67530865, compound

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

(S)-{5-[(4-cyano-benzenesulfonyl)-isobutyl-amino]-6-hydroxy-hexyl}-carbamic acid tert-butyl ester (5) (1.06 g) was dissolved in 50 mL MeOH. HCl (5-6 N in i-prOH, 30 mL) was added and the mixture was stirred overnight at RT. The mixture was evaporated to dryness and used as such in the next reaction.

Workup

  • customThe mixture was evaporated to dryness
  • customsuch in the next reaction
  • Sources & evidence

    ORD record
    ord-3ba22c5e85434291af45aef527c17cf7
    Source dataset
    uspto-grants-2012_11
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US08318779B2

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes