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

Dichloromethane → HCID 89964896, compound

HRID 1846226
Notes
Print preview

Reaction equation

HRID 1846226 reaction equation
[NH:1]1[C:10]2[C:5](=[N:6][CH:7]=[CH:8][CH:9]=2)[C:4](=[O:11])[CH2:3][CH2:2]1.C(Cl)Cl.CCN(C(C)C)C(C)C.[C:24](Cl)(=[O:26])[CH3:25]>>[C:24]([N:1]1[C:10]2[C:5](=[N:6][CH:7]=[CH:8][CH:9]=2)[C:4](=[O:11])[CH2:3][CH2:2]1)(=[O:26])[CH3:25]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 4

HCID 6344DichloromethaneHCID 6367Acetyl chlorideHCID 81531DiisopropylethylamineHCID 54710388HCID 54710388, compound

Product 1

HCID 89964896HCID 89964896, compound

Procedure

To a solution of 2,3-dihydro-1,5-naphthyridin-4(1H)-one (1 eq.) and DCM (0.2 eq.) is added DIEA (2.2 eq.) and acetyl chloride (1.2 eq.). The reaction is monitored by TLC. The reaction is washed with water, brine, dried over MgSO4, concentrated in vacuo, and purified by column chromatography to give the title compound.

Workup

  1. washThe reaction is washed with water, brine
  2. dry with materialdried over MgSO4
  3. concentrationconcentrated in vacuo
  4. custompurified by column chromatography

Sources & evidence

ORD record
ord-5377103f1fb145d797477198b340832a
Source dataset
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08952009B2

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes