17-Aminoheptadecanoic acid tert-butyl ester → 15-Aminopentadecanoic acid tert-butyl ester
Reaction equation
[C:1]([O:5][C:6](=[O:24])[CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20]CCN)([CH3:4])([CH3:3])[CH3:2].C(OC(COC(C[NH:37]CC(O)=O)=O)=O)(C)(C)C>>[C:1]([O:5][C:6](=[O:24])[CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][NH2:37])([CH3:4])([CH3:3])[CH3:2]Participants
3
Procedure
15-Aminopentadecanoic acid tert-butyl ester was prepared in analogous fashion to 17-aminoheptadecanoic acid tert-butyl ester, and was coupled to (tert-butoxycarbonylmethoxycarbonylmethylamino) acetic acid in analogous fashion to the method described in Example 1, step 4.
Sources & evidence
- ORD record
- ord-9f3ebed907a349c4a214f7ee9e6a4231
- Source dataset
- uspto-grants-2014_04
- Patent number
- US08710000B2
Reaction notes
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