HRID576614

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID7972

4-Methylmorpholine

C5H11NO

结构：CC(C)(C)OC(=O)NC[C@H](NC(=O)OCc1ccccc1)C(=O)O

HCID2756240

L-N-Cbz-3-N-Boc-Amino-alanine

C16H22N2O6

结构：CN(C)C(On1nnc2cccnc21)=[N+](C)C.F[P-](F)(F)(F)(F)F

HCID9886157

Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)

C10H15F6N6OP

结构：COc1c(C[C@H](NC(=O)c2ccc(CN(C)C)c(N)c2)B2OC3CC4CC(C4(C)C)C3(C)O2)cccc1C(=O)OC(C)(C)C

HCID86725255

未命名化合物

PRODUCTS

生成物

结构：COc1c(C[C@H](NC(=O)c2ccc(CN(C)C)c(NC(=O)[C@H](CNC(=O)OC(C)(C)C)NC(=O)OCc3ccccc3)c2)B2OC3CC4CC(C4(C)C)C3(C)O2)cccc1C(=O)OC(C)(C)C

HCID86725254

未命名化合物

AUXILIARIES

试剂、催化剂与溶剂

溶剂HCID962

Water

H2O

溶剂HCID22350042

未命名化合物

PROCEDURE

实验过程

To tert-butyl 3-((2R)-2-(3-amino-4-((dimethylamino)methyl)benzamido)-2-(2,9,9-trimethyl-3,5-dioxa-4-bora-tricyclo[6.1.1.02,6]dec-4-yl)ethyl)-2-methoxybenzoate from step 3 in Example 18 (130 mg, 0.22 mol) and (S)-2-(benzyloxycarbonylamino)-3-(tert-butoxycarbonylamino)propanoic acid (85 mg, 0.25 mol) in DCM/DMF (4 mL, 1/1) was added NMM (1.2 eq) followed by HATU (114 mg, 0.3 mol). The reaction mixture was stirred overnight at rt. Water was added and the aqueous phase extracted with EtOAc. The organic phase was washed with 1N HCl, sat. NaHCO3, brine, dried and concentrated in vacuo to afford the product (0.130 g) as a brown oil. ESI-MS m/z 926.1 (MH)+.

WORKUP

后处理

extractionthe aqueous phase extracted with EtOAc
washThe organic phase was washed with 1N HCl, sat. NaHCO3, brine
customdried
concentrationconcentrated in vacuo

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-95f0cfc43fd04dc68ac6d5b49a2b5739
来源数据集: uspto-grants-2015_05
DOI: 10.6084/m9.figshare.5104873.v1
专利: US09040504B2
来源说明: uspto-grants-2015_05

反应 SMILES

[NH2:1][C:2]1[CH:3]=[C:4]([CH:38]=[CH:39][C:40]=1[CH2:41][N:42]([CH3:44])[CH3:43])[C:5]([NH:7][C@H:8]([B:25]1[O:33][CH:32]2[C:27]([CH3:37])([CH:28]3[CH2:34][CH:30]([CH2:31]2)[C:29]3([CH3:36])[CH3:35])[O:26]1)[CH2:9][C:10]1[C:11]([O:23][CH3:24])=[C:12]([CH:20]=[CH:21][CH:22]=1)[C:13]([O:15][C:16]([CH3:19])([CH3:18])[CH3:17])=[O:14])=[O:6].[CH2:45]([O:52][C:53]([NH:55][C@@H:56]([CH2:60][NH:61][C:62]([O:64][C:65]([CH3:68])([CH3:67])[CH3:66])=[O:63])[C:57](O)=[O:58])=[O:54])[C:46]1[CH:51]=[CH:50][CH:49]=[CH:48][CH:47]=1.CN1CCOCC1.CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F>C(Cl)Cl.CN(C=O)C.O>[CH2:45]([O:52][C:53]([NH:55][C@@H:56]([CH2:60][NH:61][C:62]([O:64][C:65]([CH3:68])([CH3:67])[CH3:66])=[O:63])[C:57]([NH:1][C:2]1[CH:3]=[C:4]([CH:38]=[CH:39][C:40]=1[CH2:41][N:42]([CH3:43])[CH3:44])[C:5]([NH:7][C@H:8]([B:25]1[O:33][CH:32]2[C:27]([CH3:37])([CH:28]3[CH2:34][CH:30]([CH2:31]2)[C:29]3([CH3:35])[CH3:36])[O:26]1)[CH2:9][C:10]1[C:11]([O:23][CH3:24])=[C:12]([CH:20]=[CH:21][CH:22]=1)[C:13]([O:15][C:16]([CH3:17])([CH3:18])[CH3:19])=[O:14])=[O:6])=[O:58])=[O:54])[C:46]1[CH:47]=[CH:48][CH:49]=[CH:50][CH:51]=1