Hydrochloric Acid → HCID 66763971, compound

HRID 578676Notes

Reaction equation

HRID 578676 reaction equation
C(O[C:6](=O)[N:7]([CH2:9][CH2:10][O:11][C:12]1[CH:17]=[CH:16][CH:15]=[C:14]([C:18](=[O:41])[NH:19][C:20]2[CH:25]=[CH:24][CH:23]=[C:22]([CH2:26][NH:27][C:28]3[C:37]4[C:32](=[C:33]([C:38](=[O:40])[NH2:39])[CH:34]=[CH:35][CH:36]=4)[N:31]=[CH:30][N:29]=3)[CH:21]=2)[CH:13]=1)C)(C)(C)C.Cl>O1CCOCC1>[CH3:6][NH:7][CH2:9][CH2:10][O:11][C:12]1[CH:13]=[C:14]([CH:15]=[CH:16][CH:17]=1)[C:18]([NH:19][C:20]1[CH:21]=[C:22]([CH:23]=[CH:24][CH:25]=1)[CH2:26][NH:27][C:28]1[C:37]2[C:32](=[C:33]([C:38]([NH2:39])=[O:40])[CH:34]=[CH:35][CH:36]=2)[N:31]=[CH:30][N:29]=1)=[O:41]

Participants

4

Procedure

12 mg (0.11 mmol [2-(3-{3-[(8-Carbamoyl-quinazolin-4-ylamino)-methyl]-phenylcarbamoyl}-phenoxy)-ethyl]-methyl-carbamic acid tert-butyl ester were dissolved in 2 ml dioxane and 88 μl 4 N HCl in dioxane were added. The mixture was stirred overnight, filtered and washed with dioxane.

Workup

  1. filtrationfiltered
  2. washwashed with dioxane

Sources & evidence

ORD record
ord-77b034ee00db40a88c284ba6507825de
Source dataset
uspto-grants-2015_05
Patent number
US09040560B2

Reaction notes

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