Boron Trichloride → HCID 90205696, compound
Reaction equation
C([O:5][C:6](=[O:49])[C:7]1[CH:12]=[CH:11][CH:10]=[C:9]([CH2:13][CH:14]([NH:28][C:29](=[O:46])[CH2:30][C:31]2([OH:45])[CH2:36][CH2:35][CH:34]([NH:37]C(OC(C)(C)C)=O)[CH2:33][CH2:32]2)[B:15]2[O:23]C3C(C)(C4CC(C3)C4(C)C)[O:16]2)[C:8]=1OC)(C)(C)C.B(Cl)(Cl)Cl>>[NH2:37][CH:34]1[CH2:33][CH2:32][C:31]([CH2:30][C:29]([NH:28][CH:14]2[CH2:13][C:9]3[CH:10]=[CH:11][CH:12]=[C:7]([C:6]([OH:5])=[O:49])[C:8]=3[O:23][B:15]2[OH:16])=[O:46])([OH:45])[CH2:36][CH2:35]1Participants
3
Procedure
Prepared from 3-[2-[2-(4-tert-Butoxycarbonylamino-1-hydroxy-cyclohexyl)-acetylamino]-2-(2,9,9-trimethyl-3,5-dioxa-4-bora-tricyclo[6.1.1.02,6]dec-4-yl)-ethyl]-2-methoxy-benzoic acid tert-butyl ester and BCl3 following the procedure described in Step 2 of Example 1. The crude product was purified by reverse phase preparative HPLC and dried using lyophilization. ESI-MS m/z 363 (MH)+.
Workup
- customThe crude product was purified by reverse phase preparative HPLC
- customdried
Sources & evidence
- ORD record
- ord-43b3efb4cd694a769d9839c7b68569cd
- Source dataset
- uspto-grants-2014_12
- Patent number
- US08912169B2
Reaction notes
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