allyl (1S,5R,6S)-2-(hydroxymethyl)-6-[1(R)-allyloxycarbonyloxy-ethyl]-1-methylcarbapen-2-em-3-carboxylate → HCID 178462314, compound

HRID 1603519Notes

Reaction equation

HRID 1603519 reaction equation
C(OC([O:7][C@@H:8]([C@H:10]1[C:25](=[O:26])[N:12]2[C:13]([C:19]([O:21]CC=C)=[O:20])=[C:14]([CH2:17]O)[C@H:15]([CH3:16])[C@H:11]12)[CH3:9])=O)C=C.[C:27]([C:30]1[S:34][C:33]2=[CH:35][N:36]=[CH:37][N:32]2[CH:31]=1)(=[O:29])[NH2:28]>>[OH:7][C@@H:8]([C@H:10]1[C:25](=[O:26])[N:12]2[C:13]([C:19]([O-:21])=[O:20])=[C:14]([CH2:17][N:36]3[CH:35]=[C:33]4[S:34][C:30]([C:27](=[O:29])[NH2:28])=[CH:31][N+:32]4=[CH:37]3)[C@H:15]([CH3:16])[C@H:11]12)[CH3:9]

Participants

3

Reactant 2

HCID 11046746allyl (1S,5R,6S)-2-(hydroxymethyl)-6-[1(R)-allyloxycarbonyloxy-ethyl]-1-methylcarbapen-2-em-3-carboxylateHCID 19605222HCID 19605222, compound

Product 1

HCID 178462314HCID 178462314, compoundYield 6.5%

Procedure

The same procedure as in Example 1 was repeated except that 107 mg of allyl (1S,5R,6S)-6-[(1R)-1-allyloxycarbonyloxyethyl]-2-hydroxymethyl-1-methyl-1-carbapen-2-em-3-carboxylate and 74 mg of 2-carbamoylimidazo[5,1-b]thiazole were used, thereby obtaining 7.4 mg of the title compound.

Sources & evidence

ORD record
ord-4eca68195c7045e685b0f9fbec293c11
Source dataset
uspto-grants-1999_11
Patent number
US05990101

Reaction notes

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