HCID 12543456, compound → HCID 20392477, compound

HRID 1863259Notes

Reaction equation

HRID 1863259 reaction equation
[C:1]1([CH:7]([C:9]2[O:10][CH:11]=[C:12]([CH3:14])[N:13]=2)[CH3:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.CS([C:19]1[CH2:20][O:21][CH2:22][CH:23]=1)(=O)=O>>[C:1]1([CH:7]([C:9]2[C:19]3[CH2:20][O:21][CH2:22][C:23]=3[C:11]([OH:10])=[C:12]([CH3:14])[N:13]=2)[CH3:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

Participants

3

Reactant 2

HCID 12543456HCID 12543456, compoundHCID 53761393HCID 53761393, compound

Product 1

HCID 20392477HCID 20392477, compound

Procedure

4-α-Phenylethyl-6-methyl-1,3-dihydro-furo[3,4-c]pyridin-7-ol is prepared, using the method described in Example 13, by reacting 2-α-phenylethyl-4-methyloxazole and 3-methylsulfonyl-2,5-dihydrofuran; melting point 163° C.

Sources & evidence

ORD record
ord-4b9db6a4fae24d2a92eedd54d5129be4
Source dataset
uspto-grants-1979_09
Patent number
US04168379

Reaction notes

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