Hydrochloric Acid → HCID 178491870, compound

HRID 1486183Notes

Reaction equation

HRID 1486183 reaction equation
C([O:5][C:6](=[O:48])[C:7]1[CH:12]=[CH:11][CH:10]=[C:9]([CH2:13][C@H:14]([NH:28][C:29](=[O:45])[CH2:30][C@H:31]2[CH2:36][CH2:35][C@H:34]([NH:37]C(OC(C)(C)C)=O)[CH2:33][CH2:32]2)[B:15]2[O:23][CH:22]3[C:17]([CH3:27])([CH:18]4[CH2:24][CH:20]([CH2:21]3)[C:19]4([CH3:26])[CH3:25])[O:16]2)[C:8]=1[O:46][CH3:47])(C)(C)C.Cl.C(OCC)C>O1CCOCC1>[NH2:37][C@H:34]1[CH2:35][CH2:36][C@H:31]([CH2:30][C:29]([NH:28][C@H:14]([B:15]2[O:23][CH:22]3[C:17]([CH3:27])([CH:18]4[CH2:24][CH:20]([CH2:21]3)[C:19]4([CH3:26])[CH3:25])[O:16]2)[CH2:13][C:9]2[C:8]([O:46][CH3:47])=[C:7]([CH:12]=[CH:11][CH:10]=2)[C:6]([OH:48])=[O:5])=[O:45])[CH2:32][CH2:33]1

Participants

5

Procedure

To tert-butyl 3-((2R)-2-(2-(tran-4-(tert-butoxycarbonylamino)cyclohexyl)acetamido)-2-(2,9,9-trimethyl-3,5-dioxa-4-bora-tricyclo[6.1.1.02,6]dec-4-yl)ethyl)-2-methoxybenzoate from Step 1 of Example 6 (640 mg) was added 4 N HCl in dioxane (4 mL). The resultant reaction mixture was stirred at RT for 1 hr. Diethyl ether was added to precipitate out the product as while solid (500 mg) which was used directly to the next step.

Workup

  1. customThe resultant reaction mixture
  2. customto precipitate out the product as while solid (500 mg) which

Sources & evidence

ORD record
ord-3d71d947f2014f2ba4cc80b725b169af
Source dataset
uspto-grants-2016_08
Patent number
US09422314B2

Reaction notes

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