HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

Hydrochloric Acid → HCID 69692374, compound

HRID 277199
Notes
Print preview

Reaction equation

HRID 277199 reaction equation
[CH2:1]([O:3][C:4](=[O:26])[CH2:5][C:6]([C:8]1[O:12][N:11]=[C:10]([CH:13]([NH:18]C(OC(C)(C)C)=O)[CH2:14][CH:15]([CH3:17])[CH3:16])[CH:9]=1)=[O:7])[CH3:2].[ClH:27]>O1CCOCC1>[ClH:27].[CH2:1]([O:3][C:4](=[O:26])[CH2:5][C:6]([C:8]1[O:12][N:11]=[C:10]([CH:13]([NH2:18])[CH2:14][CH:15]([CH3:16])[CH3:17])[CH:9]=1)=[O:7])[CH3:2]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 313Hydrochloric AcidHCID 18682354HCID 18682354, compound

Product 1

HCID 69692374HCID 69692374, compound

Reagents, catalysts & solvents 1

HCID 312751,4-DioxaneSolvent

Procedure

A solution of 3-[3-(1-tert-butoxycarbonylamino-3-methyl-butyl)-isoxazol-5-yl]-3-oxo-propionic acid ethyl ester (1.4 g, 3.9 mmol) in 4M HCl in dioxane (5 ml) was stirred at room temperature. After 3 h the mixture was concentrated under reduced pressure to give the title compound as a pale yellow solid. MS [M+1]+269.0.

Workup

  • concentrationAfter 3 h the mixture was concentrated under reduced pressure
  • Sources & evidence

    ORD record
    ord-3b449bc0b4fc4a8d87db93878082bcf2
    Source dataset
    uspto-grants-2002_03
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US06355662B1

    Reaction notes

    Loading…

    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes