Hydrochloric Acid → HCID 44599584, compound

HRID 1048049Notes

Reaction equation

HRID 1048049 reaction equation
C(OC([N:8]1[CH2:17][CH2:16][C:15]2[C:10](=[CH:11][C:12]([NH:18][C:19]([C:21]3[CH:42]=[CH:41][C:24]([O:25][C:26]4[CH:35]=[C:34]5[C:29]([CH:30]([C:36]([OH:38])=[O:37])[CH2:31][CH2:32][O:33]5)=[CH:28][C:27]=4[C:39]#[N:40])=[CH:23][CH:22]=3)=[O:20])=[CH:13][CH:14]=2)[CH2:9]1)=O)(C)(C)C.[ClH:43]>O1CCOCC1>[ClH:43].[C:39]([C:27]1[CH:28]=[C:29]2[C:34](=[CH:35][C:26]=1[O:25][C:24]1[CH:23]=[CH:22][C:21]([C:19](=[O:20])[NH:18][C:12]3[CH:11]=[C:10]4[C:15]([CH2:16][CH2:17][NH:8][CH2:9]4)=[CH:14][CH:13]=3)=[CH:42][CH:41]=1)[O:33][CH2:32][CH2:31][CH:30]2[C:36]([OH:38])=[O:37])#[N:40]

Participants

4

Procedure

To a stirred solution of 7-(4-(2-(tert-butoxycarbonyl)-1,2,3,4-tetrahydroisoquinolin-7-ylcarbamoyl)phenoxy)-6-cyanochroman-4-carboxylic acid (40 mg, 0.070 mmol) in dioxane (1 mL) at ambient temperature was added a 4M solution of hydrogen chloride in dioxane (2 mL). The resulting solution was stirred at ambient temperature for 90 minutes. Some dark material had separated from the cloudy reaction mixture, and the supernatant was concentrated to afford 6-cyano-7-(4-(1,2,3,4-tetrahydroisoquinolin-7-ylcarbamoyl)phenoxy)chroman-4-carboxylic acid hydro-chloride as a light tan solid (30 mg, 84% yield). MS (apci) m/z=470.2 (M−Cl).

Workup

  1. customSome dark material had separated from the cloudy reaction mixture
  2. concentrationthe supernatant was concentrated

Sources & evidence

ORD record
ord-6deea1f06b8b42b0aafcd8bcefeee7e2
Source dataset
uspto-grants-2013_10
Patent number
US08569522B2

Reaction notes

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