Boron Trichloride → HCID 76903250, 화합물
반응식
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])[CH:30]=[C:31]2[CH2:36][CH2:35][CH:34]([CH2:37][NH:38]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>>[NH2:38][CH2:37][CH:34]1[CH2:35][CH2:36][C:31](=[CH:30][C:29]([NH:28][C@H: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])[CH2:32][CH2:33]1참가 물질
3
실험 절차
Prepared from 3-[2-{2-[4-(tert-Butoxycarbonylamino-methyl)-cyclohexylidene]-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 359 (MH)+.
후처리
- customThe crude product was purified by reverse phase preparative HPLC
- customdried
출처 및 근거
- ORD 기록
- ord-f26c92afa4ba41ff96c3737848d96e4e