Oxalyl chloride → HCID 57732770, compound

HRID 1806485Notes

Reaction equation

HRID 1806485 reaction equation
[O:1]1[CH2:5][CH2:4][CH:3]([C:6]([OH:8])=O)[CH2:2]1.C(Cl)(=O)C(Cl)=O.[NH2:15][CH2:16][C:17]1[CH:18]=[C:19]([C:23]2[CH:24]=[C:25]3[C:29](=[C:30]([C:32]([NH2:34])=[O:33])[CH:31]=2)[NH:28][CH:27]=[C:26]3[CH:35]2[CH2:40][CH2:39][N:38]([S:41]([CH2:44][CH3:45])(=[O:43])=[O:42])[CH2:37][CH2:36]2)[CH:20]=[CH:21][CH:22]=1.CCN(C(C)C)C(C)C>C(Cl)Cl.N1C=CC=CC=1.CN(C=O)C>[CH2:44]([S:41]([N:38]1[CH2:39][CH2:40][CH:35]([C:26]2[C:25]3[C:29](=[C:30]([C:32]([NH2:34])=[O:33])[CH:31]=[C:23]([C:19]4[CH:20]=[CH:21][CH:22]=[C:17]([CH2:16][NH:15][C:6]([CH:3]5[CH2:4][CH2:5][O:1][CH2:2]5)=[O:8])[CH:18]=4)[CH:24]=3)[NH:28][CH:27]=2)[CH2:36][CH2:37]1)(=[O:43])=[O:42])[CH3:45]

Participants

8

Reactant 4

HCID 65578Oxalyl chlorideHCID 81531DiisopropylethylamineHCID 4661317(R)-Tetrahydro-3-furoic acidHCID 16038109HCID 16038109, compound

Product 1

HCID 57732770HCID 57732770, compoundYield 10.2%

Reagents, catalysts & solvents 3

HCID 1049PyridineCatalystHCID 6228DimethylformamideSolventHCID 6344DichloromethaneSolvent

Procedure

To a solution of tetrahydro-3-furancarboxylic acid (17 mg, 0.144 mmol) in DCM (2.0 mL) was added pyridine (3 drops) and oxalyl chloride (18 mg, 0.144 mmol). Reaction mixture was stirred overnight at room temperature. To the mixture was then added 5-[3-(aminomethyl)phenyl]-3-[1-(ethylsulfonyl)-4-piperidinyl]-1H-indole-7-carboxamide (40 mg, 0.096 mmol) in DMF (1.0 mL) and DIEA (33 μL, 0.192 mmol). Reaction mixture was stirred at room temperature overnight. Reaction mixture was concentrated under nitrogen and purified by Gilson Preparatory HPLC to give 5.3 mg the title compound (10%).

Workup

  1. customReaction mixture
  2. customReaction mixture
  3. stirringwas stirred at room temperature overnight
  4. customReaction mixture
  5. concentrationwas concentrated under nitrogen
  6. custompurified by Gilson Preparatory HPLC

Sources & evidence

ORD record
ord-fcd342de0dea4c0e97c422e62a3e0ef2
Source dataset
uspto-grants-2013_01
Patent number
US08354406B2

Reaction notes

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