Water → HCID 76902876, compound

HRID 1486191Notes

Reaction equation

HRID 1486191 reaction equation
[C:1]([N:8]1[CH:12]=[CH:11][N:10]=C1)([N:3]1[CH:7]=[CH:6][N:5]=[CH:4]1)=[O:2].[NH2:13][CH2:14][CH2:15][NH:16][C:17](=[O:23])OC(C)(C)C.NCCNC1[CH2:31][CH:30]([CH2:32][C:33]([NH:35][C@H:36]([B:49]2[O:57]C3C(C)(C4CC(C3)C4(C)C)[O:50]2)[CH2:37][C:38]2[C:39](OC)=[C:40]([CH:44]=[CH:45][CH:46]=2)[C:41]([OH:43])=[O:42])=[O:34])[CH2:29]1.O>C(Cl)Cl.CN(C=O)C>[NH2:10][CH2:11][CH2:12][NH:8][C:1](=[O:2])[N:3]([CH:4]1[CH2:29][CH:30]([CH2:32][C:33]([NH:35][C@H:36]2[CH2:37][C:38]3[CH:46]=[CH:45][CH:44]=[C:40]([C:41]([OH:43])=[O:42])[C:39]=3[O:57][B:49]2[OH:50])=[O:34])[CH2:31]1)[CH2:7][CH2:6][NH:5][C:17]([NH:16][CH2:15][CH2:14][NH2:13])=[O:23]

Participants

7

Procedure

To 1,1′-Carbonyldiimidazole (180 mg) in DCM (5 mL) was added tert-butyl 2-aminoethylcarbamate (160 mg). The resultant reaction mixture was stirred at RT for 1 hr. A portion of this solution (1 mL) was then added to 3-((2R)-2-(2-(3-(2-aminoethylamino)cyclobutyl)acetamido)-2-(2,9,9-trimethyl-3,5-dioxa-4-bora-tricyclo[6.1.1.02,6]dec-4-yl)ethyl)-2-methoxybenzoic acid from step 1 (20 mg) in DMF and TEA (2 eq) in a different flask. The reaction mixture was stirred overnight. Water was added and extracted with EtOAc. The combine organic phases were dried and concentrated in vacuo to afford the product which was used directly to next step.

Workup

  1. customThe resultant reaction mixture
  2. stirringThe reaction mixture was stirred overnight
  3. extractionextracted with EtOAc
  4. customThe combine organic phases were dried
  5. concentrationconcentrated in vacuo
  6. customto afford the product which

Sources & evidence

ORD record
ord-337706f90c074ab29d544b99603155f3
Source dataset
uspto-grants-2016_08
Patent number
US09422314B2

Reaction notes

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