Hydrochloric Acid → HCID 178524378, compound

HRID 1919653Notes

Reaction equation

HRID 1919653 reaction equation
[NH:1]1[C:5]([C:6]2[CH:7]=[CH:8][C:9]3[C:10]4[S:30][CH:29]=[CH:28][C:11]=4[C:12]([NH:16][C:17]4[CH:18]=[C:19]([CH:25]=[CH:26][CH:27]=4)[C:20]([O:22]CC)=[O:21])=[N:13][C:14]=3[CH:15]=2)=[N:4][N:3]=[N:2]1.C1COCC1.[OH-].[Li+].Cl>O.CO>[NH:1]1[C:5]([C:6]2[CH:7]=[CH:8][C:9]3[C:10]4[S:30][CH:29]=[CH:28][C:11]=4[C:12]([NH:16][C:17]4[CH:18]=[C:19]([CH:25]=[CH:26][CH:27]=4)[C:20]([OH:22])=[O:21])=[N:13][C:14]=3[CH:15]=2)=[N:4][N:3]=[N:2]1

Participants

7

Procedure

ethyl 3-(7-(1H-tetrazol-5-yl)thieno[3,2-c]quinolin-4-ylamino)benzoate (1.0 eq, 7.6 mg, 0.018 mmol) was suspended in a 1:1:1 mixture of THF, MeOH and water. Lithium Hydroxide was added (40 mg, 1.66 mmol) and the mixture stirred at room temperature for one hour. Water and hydrochloric acid were added and the resulting solid filtered and dried to afford 3-(7-(1H-tetrazol-5-yl)thieno[3,2-c]quinolin-4-ylamino)benzoic acid as a solid. LCMS (ES): 95% pure, m/z 389 [M+1]+.

Workup

  1. filtrationthe resulting solid filtered
  2. customdried

Sources & evidence

ORD record
ord-fadefebc8de44c739fa3a4b0f12af03b
Source dataset
uspto-grants-2012_05
Patent number
US08168651B2

Reaction notes

Loading…