Acetic Anhydride → HCID 67050629, compound

HRID 1190629Notes

Reaction equation

HRID 1190629 reaction equation
[Br:1][C:2]1[CH:3]=[CH:4][C:5]2[C:11]3[S:12][C:13]([C:15]([N:17]([C:19]4[CH:24]=[C:23]([C:25](=[O:30])[NH:26][CH2:27][CH2:28][OH:29])[CH:22]=[CH:21][C:20]=4[Cl:31])[CH3:18])=[O:16])=[CH:14][C:10]=3[CH2:9][CH2:8][O:7][C:6]=2[CH:32]=1.[C:33](OC(=O)C)(=[O:35])[CH3:34]>N1C=CC=CC=1>[C:33]([O:29][CH2:28][CH2:27][NH:26][C:25](=[O:30])[C:23]1[CH:22]=[CH:21][C:20]([Cl:31])=[C:19]([N:17]([CH3:18])[C:15]([C:13]2[S:12][C:11]3[C:5]4[CH:4]=[CH:3][C:2]([Br:1])=[CH:32][C:6]=4[O:7][CH2:8][CH2:9][C:10]=3[CH:14]=2)=[O:16])[CH:24]=1)(=[O:35])[CH3:34]

Participants

4

Reactant 2

HCID 7918Acetic AnhydrideHCID 67050562HCID 67050562, compound

Product 1

HCID 67050629HCID 67050629, compoundYield 83.5%

Reagents, catalysts & solvents 1

HCID 1049PyridineSolvent

Conditions

Temperature
0 °C

Procedure

8-Bromo-N-(2-chloro-5-(2-hydroxyethylcarbamoyl)phenyl)-N-methyl-4,5-dihydrobenzo[b]thieno[2,3-d]oxepine-2-carboxamide (0.5 g, 0.933 mmol) was dissolved in 5 mL of pyridine. The mixture was stirred at 0° C. and acetic anhydride (0.2 g, 2 eq) was added dropwise. It was stirred at room temperature for overnight. The mixture was poured into ice water and the mixture was extracted by DCM. The combined organics were dried and evaporated in vacuum to afford the acetylated product, 2-(3-(8-bromo-N-methyl-4,5-dihydrobenzo[b]thieno[2,3-d]oxepine-2-carboxamido)-4-chlorobenzamido)ethyl acetate (0.45 g, yield: 83%). LC-MS: (ESI, m/z)=577 [M+H]+

Workup

  1. stirringIt was stirred at room temperature for overnight
  2. extractionthe mixture was extracted by DCM
  3. customThe combined organics were dried
  4. customevaporated in vacuum

Sources & evidence

ORD record
ord-f05270cce3814cc886bb019ee1a95bbc
Source dataset
uspto-grants-2014_03
Patent number
US08673952B2

Reaction notes

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