Sodium Hydroxide → HCID 145857659, compound

HRID 2216118Notes

Reaction equation

HRID 2216118 reaction equation
C[O:2][C:3](=[O:48])[CH2:4][NH:5][C:6]([NH:8][CH2:9][CH2:10][NH:11][C:12]([NH:14][C:15]1[CH:20]=[CH:19][CH:18]=[C:17]([CH3:21])[C:16]=1[C:22]1[CH:27]=[CH:26][CH:25]=[C:24]([S:28]([C:31]2[CH:35]=[C:34]([C:36]([NH:38][C:39]([O:41][C:42]([CH3:45])([CH3:44])[CH3:43])=[O:40])=[NH:37])[S:33][C:32]=2[S:46][CH3:47])(=[O:30])=[O:29])[CH:23]=1)=[O:13])=[O:7].[OH-].[Na+]>CO.O>[C:42]([O:41][C:39]([NH:38][C:36](=[NH:37])[C:34]1[S:33][C:32]([S:46][CH3:47])=[C:31]([S:28]([C:24]2[CH:23]=[C:22]([C:16]3[C:17]([CH3:21])=[CH:18][CH:19]=[CH:20][C:15]=3[NH:14][C:12](=[O:13])[NH:11][CH2:10][CH2:9][NH:8][C:6](=[O:7])[NH:5][CH2:4][C:3]([OH:48])=[O:2])[CH:27]=[CH:26][CH:25]=2)(=[O:30])=[O:29])[CH:35]=1)=[O:40])([CH3:45])([CH3:43])[CH3:44]

Participants

4

Procedure

A solution of {3-[2-(3-{3′-[5-(tert-butoxycarbonylamino-imino-methyl)-2-methylsulfanyl-thiophene-3-sulfonyl]-6-methyl-biphenyl-2-yl}-ureido)-ethyl]-ureido}-acetic acid methyl ester ((Example 197: step a) 0.031 g, 0.042 mmol) in MeOH:water (2:1, 15 mL) was treated with NaOH (10 N, 0.042 mL, 0.420 mmol) and stirred at room temperature 18 h. MeOH was evaporated in vacuo and the remaining aqueous solution was acidified to pH 5 with glacial acetic acid. The solution was extracted with CH2Cl2 (3×50 mL). The combined organic layers were dried over MgSO4 and evaporated in vacuo to afford the product {3-[2-(3-{3′-[5-(tert-butoxycarbonylamino-imino-methyl)-2-methylsulfanyl-thiophene-3-sulfonyl]-6-methyl-biphenyl-2-yl}-ureido)-ethyl]-ureido}-acetic acid (0.025 g, 83%) as an off-white solid. The crude material was used directly in the next reaction.

Workup

  1. customMeOH was evaporated in vacuo
  2. extractionThe solution was extracted with CH2Cl2 (3×50 mL)
  3. dry with materialThe combined organic layers were dried over MgSO4
  4. customevaporated in vacuo

Sources & evidence

ORD record
ord-41b8e5affe374d9d82570f395b50219e
Source dataset
uspto-grants-2006_09
Patent number
US07109354B2

Reaction notes

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