Hydrochloric Acid → HCID 69217912, compound
Reaction equation
[ClH:1].[CH2:2]([O:9][C:10](=[O:57])[NH:11][CH2:12][CH2:13][NH:14][C:15](=[O:56])[C@@H:16]([NH:30][C:31](=[O:55])[C@H:32]([CH2:41][CH2:42][CH2:43][NH:44][C:45]([O:47]CC1C=CC=CC=1)=[O:46])[NH:33]C(OC(C)(C)C)=O)[CH2:17][CH2:18][NH:19][C:20]([O:22][CH2:23][C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1)=[O:21])C1C=CC=CC=1.O1[CH2:63][CH2:62]OCC1>>[ClH:1].[CH2:23]([N:44]([CH2:43][CH2:42][CH2:41][C@H:32]([NH2:33])[C:31](=[O:55])[NH:30][C@@H:16]([CH2:17][CH2:18][NH:19][C:20]([O:22][CH2:23][C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1)=[O:21])[C:15](=[O:56])[NH:14][CH2:13][CH2:12][NH:11][C:10](=[O:57])[O:9][CH2:2][C:63]1[CH:62]=[CH:15][CH:16]=[CH:17][CH:18]=1)[C:45](=[O:46])[OH:47])[C:24]1[CH:25]=[CH:26][CH:27]=[CH:28][CH:29]=1Participants
4
Procedure
3.7 ml of a 4M solution of hydrogen chloride in dioxane are added to a solution of 71 mg (0.091 mmol) of benzyl{2-[((2S)-4-{[(benzyloxy)carbonyl]amino}-2-{[N5-[(benzyloxy)carbonyl]-N2-(tert-butoxycarbonyl)-L-ornithyl]amino}butanoyl)amino]ethyl}carbamate (Example 112A) in 1.5 ml of dioxane at RT. After 4 h at RT, the reaction solution is concentrated in vacuo, coevaporated with dichloromethane several times and dried under high vacuum. The crude product is reacted without further purification.
Workup
- concentrationthe reaction solution is concentrated in vacuo
- customdried under high vacuum
- customThe crude product is reacted without further purification
Sources & evidence
- ORD record
- ord-7b992cdf4c68460e9183723e1270ec58
- Source dataset
- uspto-grants-2008_11
- Patent number
- US07446102B2
Reaction notes
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