Sodium Hydroxide → HCID 178448443, compound

HRID 267120Notes

Reaction equation

HRID 267120 reaction equation
[N:1]#[N:2].[CH2:3]([O:10][C:11]([NH:13][C@H:14]([C:31]([NH:33][C@@H:34]([CH2:50][C:51]1[CH:56]=[CH:55][CH:54]=[CH:53][CH:52]=1)[C@H:35]([OH:49])[CH2:36][C@@:37]1([C:46]([NH2:48])=[O:47])[CH2:41][CH2:40][CH2:39][N:38]1[C:42]([CH3:45])([CH3:44])[CH3:43])=[O:32])[CH2:15][C:16]1[N:20](C(OCC2C=CC=CC=2)=O)[CH:19]=[N:18][CH:17]=1)=[O:12])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[OH-].[Na+]>Cl>[N:1]#[N:2].[CH2:3]([O:10][C:11]([NH:13][C@H:14]([C:31]([NH:33][C@@H:34]([CH2:50][C:51]1[CH:52]=[CH:53][CH:54]=[CH:55][CH:56]=1)[C@H:35]([OH:49])[CH2:36][C@@:37]1([C:46]([NH2:48])=[O:47])[CH2:41][CH2:40][CH2:39][N:38]1[C:42]([CH3:45])([CH3:44])[CH3:43])=[O:32])[CH2:15][C:16]1[N:20]=[CH:19][NH:18][CH:17]=1)=[O:12])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1

Participants

4

Procedure

A solution of 30 mg of N2 -[3(S)-[[N,3-bis(benzyloxycarbonyl)-L-histidyl]amino]-2(R)-hydroxy-4-phenylbutyl]-N1 -tert.butyl-L-prolinamide in 6 ml of 2M hydrochloric acid was stirred at room temperature overnight. The mixture was neutralized by the addition of 2M sodium hydroxide solution and extracted with two 10 ml portions of dichloromethane. The combined extracts were dried over anhydrous sodium sulphate and evaporated. The crude product was triturated with diethyl ether to give 14 mg of N2 -[3(S)-[[N-(benzyloxycarbonyl)-L-histidyl]amino]-2(R)-hydroxy-4-phenylbutyl]-N1 -tert.butyl-L-prolinamide as a white solid of melting point 100° C. (decomposition); MS: m/e 604 [M]+.

Workup

  1. extractionextracted with two 10 ml portions of dichloromethane
  2. dry with materialThe combined extracts were dried over anhydrous sodium sulphate
  3. customevaporated
  4. customThe crude product was triturated with diethyl ether

Sources & evidence

ORD record
ord-4b016298dab34cb089f8b56ff0bfcce9
Source dataset
uspto-grants-1997_07
Patent number
US05652369

Reaction notes

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