Benzyl chloroformate → HCID 54567698, compound
Reaction equation
Br.Br.[C:3]1([CH3:21])[CH:8]=[CH:7][C:6]([S:9]([N:12]2[CH2:20][CH2:19][NH:18][CH2:17][CH2:16][NH:15][CH2:14][CH2:13]2)(=[O:11])=[O:10])=[CH:5][CH:4]=1.[C:22]([O-:25])([O-:24])=O.[K+].[K+].Cl[C:29]([O:31][CH2:32][C:33]1[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=1)=[O:30]>>[C:3]1([CH3:21])[CH:4]=[CH:5][C:6]([S:9]([N:12]2[CH2:13][CH2:14][N:15]([C:22]([O:25][CH2:21][C:3]3[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=3)=[O:24])[CH2:16][CH2:17][N:18]([C:29]([O:31][CH2:32][C:33]3[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=3)=[O:30])[CH2:19][CH2:20]2)(=[O:10])=[O:11])=[CH:7][CH:8]=1Participants
4
Procedure
From N-(p-toluenesulfonyl)-1,4,7-triazacyclononane dihydrobromide (1.3.13.31), K2CO3 and benzyl chloroformate.
Sources & evidence
- ORD record
- ord-1e8cbf4e4f454ddb9e8914f3ddafabfe
- Source dataset
- uspto-grants-2002_05
- Patent number
- US06387891B2
Reaction notes
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