Benzene → HCID 15617948, compound

HRID 1762664Notes

Reaction equation

HRID 1762664 reaction equation
[C:1](Cl)(=[O:5])[C:2](Cl)=O.[CH:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1.[NH:13]1[CH2:17][CH2:16][CH2:15][CH2:14]1.CC[O:20][CH2:21][CH3:22]>C(Cl)Cl>[OH:20][C:21]1[C:22]2[C:9](=[CH:8][CH:7]=[CH:12][CH:11]=2)[CH:7]=[CH:12][C:11]=1[CH2:10][CH2:9][CH2:8][CH2:2][C:1]([N:13]1[CH2:17][CH2:16][CH2:15][CH2:14]1)=[O:5]

Participants

6

Reactant 4

HCID 241BenzeneHCID 3283Diethyl EtherHCID 31268PyrrolidineHCID 65578Oxalyl chloride

Product 1

HCID 15617948HCID 15617948, compoundYield 76%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

A mixture of the compound of Example 131 Part B (1.00 g, 3.0 mmole), oxalyl chloride (1.3 mL, 15.0 mmole) and benzene (10 mL) was stirred at room temperature for 21 hours and concentrated under vacuum. The residue was dissolved in methylene chloride (10 mL) and added dropwise to a stirred solution of pyrrolidine (0.53 mL, 6.3 mmole) in methylene chloride (10 mL) at 0°. After 6.5 hours, the mixture was diluted with ether, washed with water and 1.0N hydrochloric acid, then dried over magnesium sulfate and concentrated under vacuum. The crude material was hydrogenated using the procedure of Example 86. Recrystallization of the crude product (ethyl acetate/ethanol) provided the title compound (0.63 g, 76%) as an off-white solid, mp 166°-160°.

Workup

  1. concentrationconcentrated under vacuum
  2. dissolutionThe residue was dissolved in methylene chloride (10 mL)
  3. waitAfter 6.5 hours
  4. washwashed with water and 1.0N hydrochloric acid
  5. dry with materialdried over magnesium sulfate
  6. concentrationconcentrated under vacuum
  7. customRecrystallization of the crude product (ethyl acetate/ethanol)

Sources & evidence

ORD record
ord-558d91ace7874eef8031c851d73ac433
Source dataset
uspto-grants-1989_05
Patent number
US04833164

Reaction notes

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