Thionyl Chloride → 2-(S)-(4-Chloromethyl-1H-indazol-5-ylmethyl)-succinic acid dimethyl ester hydrochoride

HRID 132392Notes

Reaction equation

HRID 132392 reaction equation
S(Cl)([Cl:3])=O.[CH3:5][O:6][C:7](=[O:26])[C@@H:8]([CH2:14][C:15]1[C:16]([CH2:24]O)=[C:17]2[C:21](=[CH:22][CH:23]=1)[NH:20][N:19]=[CH:18]2)[CH2:9][C:10]([O:12][CH3:13])=[O:11]>ClCCl>[ClH:3].[CH3:5][O:6][C:7](=[O:26])[C@@H:8]([CH2:14][C:15]1[C:16]([CH2:24][Cl:3])=[C:17]2[C:21](=[CH:22][CH:23]=1)[NH:20][N:19]=[CH:18]2)[CH2:9][C:10]([O:12][CH3:13])=[O:11]

Participants

4

Reactant 2

HCID 24386Thionyl ChlorideHCID 597318712-(S)-(4-Hydroxymethyl-1H-indazol-5-ylmethyl)-succinic acid dimethyl ester

Product 1

HCID 673178982-(S)-(4-Chloromethyl-1H-indazol-5-ylmethyl)-succinic acid dimethyl ester hydrochorideYield 96%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

Thionyl chloride (5.0 mL) was added to a solution of 2-(S)-(4-hydroxymethyl-1H-indazol-5-ylmethyl)-succinic acid dimethyl ester (1.53 g, 5.0 mmol) in dichloromethane (30 mL). Reaction mixture was stirred at ambient temperature for 2 hours. Mixture was concentrated in vacuo. Residue was triturated in toluene (30 mL), then concentrated in vacuo. Residue was treated with dichloromethane (30 mL) then concentrated in vacuo. Desired product was obtained in 96% yield as an orange solid. 1H NMR (300 MHz, CDCl3): δ=8.22 (s, 1H), 7.49 (d, J=8.8, 1H), 7.15 (d, J=8.8, 1H), 5.12 (s, 2H), 3.56 (s, 3H), 3.52 (s, 3H), 3.05 (m, 3H), 2.69 (dd, J1=8.1, J2=16.5), 2.54 (m, 1H). MS m/e (M+H)+=325.2.

Workup

  1. customReaction mixture
  2. concentrationMixture was concentrated in vacuo
  3. customResidue was triturated in toluene (30 mL)
  4. concentrationconcentrated in vacuo
  5. additionResidue was treated with dichloromethane (30 mL)
  6. concentrationthen concentrated in vacuo

Sources & evidence

ORD record
ord-fa942bf019ca48b59f2b413d99414a5e
Source dataset
uspto-grants-2008_06
Patent number
US07384931B2

Reaction notes

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