Hydrochloric Acid → N,N-dimethyl-[5-[4-(3,5-dichlorobenzoyl)benzoyl]-4,5,6,7-tetrahydrofuro[3,2-c]pyridin-2-ylmethyl]amine hydrochloride

HRID 611295Notes

Reaction equation

HRID 611295 reaction equation
[CH3:1][N:2]([CH2:4][C:5]1[O:13][C:12]2[CH2:11][CH2:10][N:9]([C:14](=[O:31])[C:15]3[CH:20]=[CH:19][C:18]([C:21](=[O:30])[C:22]4[CH:27]=[C:26]([Cl:28])[CH:25]=[C:24]([Cl:29])[CH:23]=4)=[CH:17][CH:16]=3)[CH2:8][C:7]=2[CH:6]=1)[CH3:3].Cl>CO.C(OCC)(=O)C>[ClH:28].[CH3:3][N:2]([CH2:4][C:5]1[O:13][C:12]2[CH2:11][CH2:10][N:9]([C:14](=[O:31])[C:15]3[CH:20]=[CH:19][C:18]([C:21](=[O:30])[C:22]4[CH:23]=[C:24]([Cl:29])[CH:25]=[C:26]([Cl:28])[CH:27]=4)=[CH:17][CH:16]=3)[CH2:8][C:7]=2[CH:6]=1)[CH3:1]

Participants

5

Procedure

N,N-Dimethyl-[5-[4-(3,5-dichlorobenzoyl)benzoyl]-4,5,6,7-tetrahydrofuro[3,2-c]pyridin-2-ylmethyl]amine 0.200 g was dissolved in 2 ml of methanol; hydrogen chloride in ethyl acetate was added in excess, followed by stirring. This was concentrated and washed with diethyl ether to yield the desired product.

Workup

  1. concentrationThis was concentrated
  2. washwashed with diethyl ether

Sources & evidence

ORD record
ord-e17fc44dc09d40e9b3c392ae86b4eb8a
Source dataset
uspto-grants-1999_12
Patent number
US05998433

Reaction notes

Loading…