Water → HCID 19076506, compound

HRID 965546Notes

Reaction equation

HRID 965546 reaction equation
C(N(CC)CC)C.[C:8](Cl)(=[O:10])[CH3:9].[NH2:12][C:13]1([C:37]2[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=2)[C:21]2[C:16](=[CH:17][CH:18]=[C:19]([Cl:22])[CH:20]=2)[N:15]([S:23]([C:26]2[CH:31]=[CH:30][C:29]([O:32][CH3:33])=[CH:28][C:27]=2[O:34][CH3:35])(=[O:25])=[O:24])[C:14]1=[O:36].O>C(Cl)Cl>[C:8]([NH:12][C:13]1([C:37]2[CH:38]=[CH:39][CH:40]=[CH:41][CH:42]=2)[C:21]2[C:16](=[CH:17][CH:18]=[C:19]([Cl:22])[CH:20]=2)[N:15]([S:23]([C:26]2[CH:31]=[CH:30][C:29]([O:32][CH3:33])=[CH:28][C:27]=2[O:34][CH3:35])(=[O:25])=[O:24])[C:14]1=[O:36])(=[O:10])[CH3:9]

Participants

6

Procedure

0.051 g of triethylamine and then 0.04 g of acetyl chloride are added to a solution of 0.234 g of the compound obtained in EXAMPLE 1 in 2 ml of DCM and the reaction mixture is stirred for two hours at RT. It is poured into water, extracted with DCM, washed with water, dried over sodium sulfate and evaporated under vacuum to give the expected product after crystallization and recrystallization from a DCM/iso ether/ MeOH mixture. m=0.146 g. M.p.=253° C.

Workup

  1. extractionextracted with DCM
  2. washwashed with water
  3. dry with materialdried over sodium sulfate
  4. customevaporated under vacuum

Sources & evidence

ORD record
ord-7b014b89fa364687a9e9c2262af89983
Source dataset
uspto-grants-1998_06
Patent number
US05773612

Reaction notes

Loading…