Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 178497003 | HCID 178497003 | — |
| Product | HCID 178507968 | HCID 178507968 | — |
Reaction Steps
See step d) of example H2 starting from 6-amino-7-chloro-1H-benzoimidazole-5-carboxylic acid methyl ester and 2 equivalents of a solution of NaOH 1 N. The reaction is stirred for 18 hours at 70° C. After evaporation, the residue is suspended in EtOAc and H2O, then the aqueous phase is acidified to pH 2-3 with concentrated HCl. The aqueous phase is coevaporated with toluene and the crude reddish solid is used directly in the next step without further purification. LC/MS: 212/214 (M+1)+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08580785B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-5899e02312c04920b3795937fd97c7f6 |
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| Source note | uspto-grants-2013_11 |
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