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

Sulfuryl chloride → 5-(6-Methoxy-pyridin-3-yl)-4-methyl-thiophene-2-sulfonyl chloride

HRID 252258
Notes
Print preview

Reaction equation

HRID 252258 reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[S:10][CH:11]=[CH:12][C:13]=2[CH3:14])=[CH:5][N:4]=1.[Li]CCCC.[S:20](Cl)([Cl:23])(=[O:22])=[O:21]>C1COCC1.C(OCC)C.C(OCC)C.C(Cl)Cl>[CH3:1][O:2][C:3]1[N:4]=[CH:5][C:6]([C:9]2[S:10][C:11]([S:20]([Cl:23])(=[O:22])=[O:21])=[CH:12][C:13]=2[CH3:14])=[CH:7][CH:8]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 3

HCID 24648Sulfuryl chlorideHCID 112065202-Methoxy-5-(3-methyl-thiophen-2-yl)-pyridineHCID 178418339Butyllithium

Product 1

HCID 866167205-(6-Methoxy-pyridin-3-yl)-4-methyl-thiophene-2-sulfonyl chloride

Reagents, catalysts & solvents 3

HCID 3283Diethyl EtherSolvent
HCID 6344
Dichloromethane
Solvent
HCID 21868444Ether tetrahydrofuranSolvent

Conditions

Temperature
-70 °C

Procedure

2-Methoxy-5-(3-methyl-thiophen-2-yl)-pyridine (0.32 g, 1.6 mmol) was dissolved in THF/diethyl ether (10 ml, 1:1 v/v) and cooled to −70° C. BuLi (1.6M hexanes, 1 ml, 1.6 ml) was added dropwise and after a further 15 min at −70° C. the reaction mixture was added via canula to a condensed solution of SO2 (5 ml) in diethyl ether (10 ml). The yellow colored reaction mixture was slowly warmed to room temperature and stirred overnight. The reaction mixture was concentrated under reduced pressure and the residue washed with diethyl ether and dried. The crude solid (0.31 g) was suspended in dry n-hexane (7 ml), cooled using an ice bath to 0° C. and treated with a solution of sulfuryl chloride (1 M, 1.2 ml, 1.2 mmol) in CH2Cl2. The reaction mixture was slowly warmed to room temperature and analyzed (TLC) showing no starting material. Solvent was removed under reduced pressure and the crude product was purified over silica gel (n-heptane/tert.butylmethyl ether 1:9 to 1:4 v/v) to yield a white solid: 0.19 g (38%), MS: m/e 304.0 (MH+).

Workup

  1. temperatureThe yellow colored reaction mixture was slowly warmed to room temperature
  2. concentrationThe reaction mixture was concentrated under reduced pressure
  3. washthe residue washed with diethyl ether
  4. customdried
  5. temperaturecooled
  6. customto 0° C.
  7. temperatureThe reaction mixture was slowly warmed to room temperature
  8. customSolvent was removed under reduced pressure
  9. customthe crude product was purified over silica gel (n-heptane/tert.butylmethyl ether 1:9 to 1:4 v/v)
  10. customto yield a white solid

Sources & evidence

ORD record
ord-658789fe53894ce0bb445e0f1fc72f39
Source dataset
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07868030B2

Reaction notes

Loading…

On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes