Tetrahydrofuran → HCID 20381779, compound

HRID 1833402Notes

Reaction equation

HRID 1833402 reaction equation
[CH3:1][N:2]1[C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][C:7]=2[O:6][C:5]2[C:13]3[C:18]([NH:19][C:4]=2[C:3]1=[O:20])=[CH:17][CH:16]=[CH:15][CH:14]=3.[H-].[Na+].C1COCC1.[Cl:28][CH2:29][CH2:30][CH2:31][N:32]1[CH2:37][CH2:36][CH2:35][CH2:34][CH2:33]1>Cl>[ClH:28].[CH3:1][N:2]1[C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][C:7]=2[O:6][C:5]2[C:13]3[C:18]([N:19]([CH2:29][CH2:30][CH2:31][N:32]4[CH2:37][CH2:36][CH2:35][CH2:34][CH2:33]4)[C:4]=2[C:3]1=[O:20])=[CH:17][CH:16]=[CH:15][CH:14]=3

Participants

6

Reactant 4

HCID 8028TetrahydrofuranHCID 24758Sodium hydrideHCID 79625Piperidine, 1-(3-chloropropyl)-HCID 54128793HCID 54128793, compound

Product 1

HCID 20381779HCID 20381779, compound

Reagents, catalysts & solvents 1

HCID 313Hydrochloric AcidSolvent

Procedure

A mixture of 1.8g of 7-methyl-7H-indolo [3,2-b][1,5]benzoxazepin-6(5H)-one, 0.42g of 57% sodium hydride-mineral oil dispersion and 10ml of THF was refluxed for 15 min. and then treated with 4.0g of 3-chloropropylpiperidine. The mixture was refluxed for 24 hrs., diluted with 2N HCl and extracted with ether. The aqueous layer was made basic with 5% NaOH and the oil extracted with ether. The ether phase was dried and treated with dry HCl to give a white solid. The solid was recrystallized from methanol-ether to give analytical material, mp. 205°-6°.

Workup

  1. temperaturewas refluxed for 15 min.
  2. temperatureThe mixture was refluxed for 24 hrs
  3. extractionextracted with ether
  4. extractionthe oil extracted with ether
  5. dry with materialThe ether phase was dried
  6. additiontreated with dry HCl
  7. customto give a white solid
  8. customThe solid was recrystallized from methanol-ether
  9. customto give analytical material, mp. 205°-6°

Sources & evidence

ORD record
ord-ceff1b05bc45410daf11b559d55785fa
Source dataset
uspto-grants-1978_01
Patent number
US04066660

Reaction notes

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