Hydrochloric Acid → HCID 44599584, compound

HRID 1021421Notes

Reaction equation

HRID 1021421 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-6d55428b78c64d5e9f23a4e0e8d7a02d
Source dataset
uspto-grants-2014_05
Patent number
US08716498B2

Reaction notes

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