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

Imidazole → HCID 68998776, compound

HRID 749989
Notes
Print preview

Reaction equation

HRID 749989 reaction equation
Cl.[NH:2]1[CH2:7][CH2:6][CH2:5][CH2:4][C@H:3]1[CH2:8][OH:9].N1C=CN=C1.C(N(CC)CC)C.[S:22](Cl)(Cl)=[O:23]>ClCCl>[S@@:22]1(=[O:23])[N:2]2[CH2:7][CH2:6][CH2:5][CH2:4][CH:3]2[CH2:8][O:9]1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 795ImidazoleHCID 8471TriethylamineHCID 24386Thionyl ChlorideHCID 69004848(s)-Piperidin-2-ylmethanol hydrochloride

Product 1

HCID 68998776HCID 68998776, compound

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent2×

Conditions

Temperature
2.5 °C

Procedure

To a solution of (S)-1-Piperidin-2-yl-methanol hydrochloride (3.43 g, 22.63 mmol), imidazole (6.1 g, 88.72 mmol) and triethylamine (7.33 g, 72.42 mmol) in anhydrous dichloromethane (120 mL) at 0-5° C. was added a solution of thionyl chloride (3.2 g, 25.86 mmol) in anhydrous dichloromethane (10 mL) over a period of 45 min. The reaction mixture was stirred at 0-5° C. for 45 min, partitioned with H2O and the aqueous layer was extracted with dichloromethane (2×150 mL). The combined organic layer was washed with H2O, dried over Na2SO4, and concentrated in vacuo to give an orange liquid. Flash column chromatography purification (silica gel, 2% EtOAc in dichloromethane) afforded the title product as a clear, colorless liquid (1.31 g, 36%).

Workup

  1. custompartitioned with H2O
  2. extractionthe aqueous layer was extracted with dichloromethane (2×150 mL)
  3. washThe combined organic layer was washed with H2O
  4. dry with materialdried over Na2SO4
  5. concentrationconcentrated in vacuo
  6. customto give an orange liquid
  7. customFlash column chromatography purification (silica gel, 2% EtOAc in dichloromethane)

Sources & evidence

ORD record
ord-1f366e205ef541f5a2eace37186ff375
Source dataset
uspto-grants-2008_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07402684B2

Reaction notes

Loading…

On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes