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Triethylamine → HCID 76485058, compound

HRID 1599669
Notes
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Reaction equation

HRID 1599669 reaction equation
BrCCCS(Cl)(=O)=O.NCC[CH2:12][CH2:13][S:14]([NH:17][CH2:18][CH:19]1[CH2:23][CH2:22][CH2:21][N:20]1[C:24](=[O:41])[CH:25]([NH:33][C:34](=[O:40])[O:35][C:36]([CH3:39])([CH3:38])[CH3:37])[CH2:26][C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1)(=[O:16])=[O:15].[CH2:42]([N:44](CC)CC)C>ClCCl>[NH2:44][CH2:42][CH2:12][CH2:13][S:14]([NH:17][CH2:18][CH:19]1[CH2:23][CH2:22][CH2:21][N:20]1[C:24](=[O:41])[CH:25]([NH:33][C:34](=[O:40])[O:35][C:36]([CH3:37])([CH3:38])[CH3:39])[CH2:26][C:27]1[CH:28]=[CH:29][CH:30]=[CH:31][CH:32]=1)(=[O:15])=[O:16]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 8471TriethylamineHCID 2893293-Bromopropane-1-sulfonyl chlorideHCID 67846374HCID 67846374, compound

Product 1

HCID 76485058HCID 76485058, compoundYield 72%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent3×

Conditions

Temperature
-10 °C

Procedure

A solution of Part A 3-bromopropyl sulfonyl chloride (1.06 g, 4.8 mmol) in dichloromethane (5 mL) was added dropwise to a cooled (-10° C.) stirred solution of Example 6a, Part B amine (1.05 g, 3.02 mmol) and triethyl amine (1.44 mL, 9.6 mmol) in dichloromethane (15 mL), After a few minutes, a precipitate formed. The suspension was stirred at -10° C. for 2.5 hours, diluted with dichloromethane (35 mL) and washed with 1N HCl solution (2×15 mL). The dichloromethane solution was dried (MgSO4), filtered and the solvent was removed in vacuo. The crude oil was purified on silica gel (Merck, 150 mL) eluting with 50% ethyl acetate in hexane to give title compound as a white foam (1.160 g, 72%).

Workup

  1. waitAfter a few minutes
  2. customa precipitate formed
  3. washwashed with 1N HCl solution (2×15 mL)
  4. dry with materialThe dichloromethane solution was dried (MgSO4)
  5. filtrationfiltered
  6. customthe solvent was removed in vacuo
  7. customThe crude oil was purified on silica gel (Merck, 150 mL)
  8. washeluting with 50% ethyl acetate in hexane

Sources & evidence

ORD record
ord-ad2514f72cba405ead6c86388790ef77
Source dataset
uspto-grants-1998_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05741799

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes